Canonical Allele Identifier: CA403080393

Gene: TCF3

Linked Data

• dbSNP Id: rs1247569590
• gnomAD v2: 19-1650181-T-G
• gnomAD v4: 19-1650182-T-G
• MyVariant Identifiers: chr19:g.1650181T>G (hg19) ; chr19:g.1650182T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1650182T>G , CM000681.2:g.1650182T>G	GRCh38
NC_000019.9:g.1650181T>G , CM000681.1:g.1650181T>G	GRCh37
NC_000019.8:g.1601181T>G	NCBI36
NG_029953.1:g.7148A>C
NG_029953.2:g.7365A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705032.1:c.67A>C	ENSP00000516067.1:p.Ser23Arg
ENST00000705033.1:n.410A>C
ENST00000262965.12:c.67A>C MANE Select	ENSP00000262965.5:p.Ser23Arg
ENST00000587235.6:c.67A>C	ENSP00000466052.3:p.Ser23Arg
ENST00000588136.7:c.67A>C MANE Plus Clinical	ENSP00000468487.1:p.Ser23Arg
ENST00000611869.5:c.67A>C	ENSP00000480564.2:p.Ser23Arg
ENST00000262965.9:c.67A>C	ENSP00000262965.4:p.Ser23Arg
ENST00000344749.9:c.67A>C	ENSP00000344375.6:p.Ser23Arg
ENST00000395423.7:c.67A>C	ENSP00000378813.3:p.Ser23Arg
ENST00000453954.6:c.67A>C	ENSP00000396363.3:p.Ser23Arg
ENST00000586318.1:c.67A>C	ENSP00000466954.1:p.Ser23Arg
ENST00000587235.5:c.67A>C	ENSP00000466052.2:p.Ser23Arg
ENST00000588136.5:c.67A>C	ENSP00000468487.1:p.Ser23Arg
ENST00000611869.4:c.67A>C	ENSP00000480564.1:p.Ser23Arg
NM_001136139.2:c.67A>C	NP_001129611.1:p.Ser23Arg
NM_003200.3:c.67A>C	NP_003191.1:p.Ser23Arg
XM_006722852.2:c.67A>C	XP_006722915.1:p.Ser23Arg
XM_006722853.2:c.67A>C	XP_006722916.1:p.Ser23Arg
XM_006722855.2:c.67A>C	XP_006722918.1:p.Ser23Arg
XM_006722856.2:c.67A>C	XP_006722919.1:p.Ser23Arg
XM_006722857.2:c.67A>C	XP_006722920.1:p.Ser23Arg
XM_006722858.2:c.67A>C	XP_006722921.1:p.Ser23Arg
XM_011528215.1:c.67A>C	XP_011526517.1:p.Ser23Arg
XM_011528216.1:c.67A>C	XP_011526518.1:p.Ser23Arg
XM_011528217.1:c.67A>C	XP_011526519.1:p.Ser23Arg
XM_011528218.1:c.67A>C	XP_011526520.1:p.Ser23Arg
XM_011528219.1:c.67A>C	XP_011526521.1:p.Ser23Arg
XM_011528220.1:c.67A>C	XP_011526522.1:p.Ser23Arg
XM_011528221.1:c.67A>C	XP_011526523.1:p.Ser23Arg
XM_011528222.1:c.67A>C	XP_011526524.1:p.Ser23Arg
XM_011528223.1:c.67A>C	XP_011526525.1:p.Ser23Arg
XM_011528224.1:c.67A>C	XP_011526526.1:p.Ser23Arg
XM_011528225.1:c.67A>C	XP_011526527.1:p.Ser23Arg
XM_011528226.1:c.67A>C	XP_011526528.1:p.Ser23Arg
XM_011528227.1:c.67A>C	XP_011526529.1:p.Ser23Arg
XR_430150.2:n.1493A>C
XR_430151.2:n.1493A>C
XR_430152.2:n.1496A>C
XR_430153.2:n.1496A>C
NM_001136139.3:c.67A>C	NP_001129611.1:p.Ser23Arg
NM_001351778.1:c.67A>C	NP_001338707.1:p.Ser23Arg
NM_001351779.1:c.67A>C	NP_001338708.1:p.Ser23Arg
NM_003200.4:c.67A>C	NP_003191.1:p.Ser23Arg
XM_006722855.4:c.67A>C	XP_006722918.1:p.Ser23Arg
XM_006722857.4:c.67A>C	XP_006722920.1:p.Ser23Arg
XM_006722858.3:c.67A>C	XP_006722921.1:p.Ser23Arg
XM_011528216.2:c.67A>C	XP_011526518.1:p.Ser23Arg
XM_011528219.2:c.67A>C	XP_011526521.1:p.Ser23Arg
XM_011528220.2:c.67A>C	XP_011526522.1:p.Ser23Arg
XM_011528221.2:c.67A>C	XP_011526523.1:p.Ser23Arg
XM_011528223.3:c.67A>C	XP_011526525.1:p.Ser23Arg
XM_011528225.2:c.67A>C	XP_011526527.1:p.Ser23Arg
XM_011528226.2:c.67A>C	XP_011526528.1:p.Ser23Arg
XM_011528227.3:c.67A>C	XP_011526529.1:p.Ser23Arg
XM_017027177.2:c.67A>C	XP_016882666.1:p.Ser23Arg
XM_017027178.1:c.67A>C	XP_016882667.1:p.Ser23Arg
XM_017027179.2:c.67A>C	XP_016882668.1:p.Ser23Arg
XM_017027180.2:c.67A>C	XP_016882669.1:p.Ser23Arg
XM_017027181.1:c.67A>C	XP_016882670.1:p.Ser23Arg
XM_017027182.1:c.67A>C	XP_016882671.1:p.Ser23Arg
XM_024451669.1:c.67A>C	XP_024307437.1:p.Ser23Arg
XM_024451670.1:c.67A>C	XP_024307438.1:p.Ser23Arg
XM_024451671.1:c.67A>C	XP_024307439.1:p.Ser23Arg
XM_024451672.1:c.67A>C	XP_024307440.1:p.Ser23Arg
XM_024451673.1:c.67A>C	XP_024307441.1:p.Ser23Arg
XM_024451674.1:c.67A>C	XP_024307442.1:p.Ser23Arg
XM_024451675.1:c.67A>C	XP_024307443.1:p.Ser23Arg
XM_024451676.1:c.67A>C	XP_024307444.1:p.Ser23Arg
XM_024451677.1:c.67A>C	XP_024307445.1:p.Ser23Arg
XM_024451678.1:c.67A>C	XP_024307446.1:p.Ser23Arg
XM_024451679.1:c.67A>C	XP_024307447.1:p.Ser23Arg
XM_024451680.1:c.67A>C	XP_024307448.1:p.Ser23Arg
XR_001753743.2:n.227A>C
XR_001753745.1:n.228A>C
XR_001753747.1:n.228A>C
XR_002958346.1:n.228A>C
XR_002958347.1:n.228A>C
XR_002958348.1:n.229A>C
XR_002958349.1:n.230A>C
XR_002958350.1:n.230A>C
XR_002958351.1:n.230A>C
NM_001136139.4:c.67A>C MANE Plus Clinical	NP_001129611.1:p.Ser23Arg
NM_003200.5:c.67A>C MANE Select	NP_003191.1:p.Ser23Arg
NM_001351778.2:c.67A>C	NP_001338707.1:p.Ser23Arg
NM_001351779.2:c.67A>C	NP_001338708.1:p.Ser23Arg