Canonical Allele Identifier: CA346670996

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104819G>A (hg19) ; chr2:g.43877680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877680G>A , CM000664.2:g.43877680G>A	GRCh38
NC_000002.11:g.44104819G>A , CM000664.1:g.44104819G>A	GRCh37
NC_000002.10:g.43958323G>A	NCBI36
NG_008884.1:g.43717G>A
NG_008884.2:g.50739G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1876G>A MANE Select	ENSP00000272286.2:p.Gly626Arg
ENST00000272286.2:c.1876G>A	ENSP00000272286.2:p.Gly626Arg
NM_022437.2:c.1876G>A	NP_071882.1:p.Gly626Arg
XM_005264483.2:c.1873G>A	XP_005264540.1:p.Gly625Arg
XM_011533029.1:c.1888G>A	XP_011531331.1:p.Gly630Arg
XM_011533030.1:c.1885G>A	XP_011531332.1:p.Gly629Arg
XM_011533031.1:c.1660G>A	XP_011531333.1:p.Gly554Arg
XR_939707.1:n.2378G>A
NM_001357321.1:c.1873G>A	NP_001344250.1:p.Gly625Arg
XM_011533029.2:c.1888G>A	XP_011531331.1:p.Gly630Arg
XM_011533030.2:c.1885G>A	XP_011531332.1:p.Gly629Arg
XR_001738891.1:n.2392G>A
XR_939707.2:n.2392G>A
NM_022437.3:c.1876G>A MANE Select	NP_071882.1:p.Gly626Arg
NM_001357321.2:c.1873G>A	NP_001344250.1:p.Gly625Arg