Canonical Allele Identifier: CA494875574

Gene: CD19

Linked Data

• gnomAD v4: 16-28937066-G-T
• MyVariant Identifiers: chr16:g.28948387G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937066G>T , CM000678.2:g.28937066G>T	GRCh38
NC_000016.9:g.28948387G>T , CM000678.1:g.28948387G>T	GRCh37
NC_000016.8:g.28855888G>T	NCBI36
NG_007275.1:g.10128G>T , LRG_35:g.10128G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1128G>T	ENSP00000313419.4:p.Pro376=
ENST00000538922.8:c.1128G>T MANE Select	ENSP00000437940.2:p.Pro376=
ENST00000324662.7:c.1128G>T	ENSP00000313419.3:p.Pro376=
ENST00000538922.5:c.1128G>T	ENSP00000437940.1:p.Pro376=
ENST00000565089.5:n.1462G>T
ENST00000567368.1:n.268G>T
ENST00000567541.5:c.1128G>T	ENSP00000456201.1:p.Pro376=
ENST00000611258.4:c.1128G>T	ENSP00000481090.1:p.Pro376=
NM_001178098.1:c.1128G>T	NP_001171569.1:p.Pro376=
NM_001770.5:c.1128G>T , LRG_35t1:c.1128G>T	NP_001761.3:p.Pro376=
XM_006721103.2:c.861G>T	XP_006721166.1:p.Pro287=
XR_950871.1:n.1141G>T
XR_950872.1:n.1030G>T
XM_006721103.3:c.861G>T	XP_006721166.1:p.Pro287=
XM_017023893.1:c.861G>T	XP_016879382.1:p.Pro287=
XR_950871.2:n.1124G>T
NM_001178098.2:c.1128G>T	NP_001171569.1:p.Pro376=
NM_001770.6:c.1128G>T MANE Select	NP_001761.3:p.Pro376=
NM_001385732.1:c.861G>T	NP_001372661.1:p.Pro287=
NR_169755.1:n.1470G>T