Canonical Allele Identifier: CA473394625
Gene: GTF2H1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.18357488G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18335941G>A , CM000673.2:g.18335941G>A GRCh38
NC_000011.9:g.18357488G>A , CM000673.1:g.18357488G>A GRCh37
NC_000011.8:g.18314064G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265963.9:c.342G>A MANE Select ENSP00000265963.4:p.Lys114=
ENST00000265963.8:c.342G>A ENSP00000265963.4:p.Lys114=
ENST00000418116.6:n.541G>A
ENST00000453096.6:c.342G>A ENSP00000393638.2:p.Lys114=
ENST00000534641.5:c.-1-2168G>A ENSP00000435375.1:n.-1-2168G>A
ENST00000543932.5:n.755G>A
NM_001142307.1:c.342G>A NP_001135779.1:p.Lys114=
NM_005316.3:c.342G>A NP_005307.1:p.Lys114=
XM_006718208.2:c.342G>A XP_006718271.1:p.Lys114=
XM_006718208.3:c.342G>A XP_006718271.1:p.Lys114=
XM_024448457.1:c.342G>A XP_024304225.1:p.Lys114=
XM_024448458.1:c.342G>A XP_024304226.1:p.Lys114=
NM_005316.4:c.342G>A MANE Select NP_005307.1:p.Lys114=
NM_001142307.2:c.342G>A NP_001135779.1:p.Lys114=