Canonical Allele Identifier: CA346663695

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43846302-G-A
• MyVariant Identifiers: chr2:g.44073441G>A (hg19) ; chr2:g.43846302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846302G>A , CM000664.2:g.43846302G>A	GRCh38
NC_000002.11:g.44073441G>A , CM000664.1:g.44073441G>A	GRCh37
NC_000002.10:g.43926945G>A	NCBI36
NG_008884.1:g.12339G>A
NG_008884.2:g.19361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.313G>A MANE Select	ENSP00000272286.2:p.Gly105Arg
ENST00000643284.1:n.770G>A
ENST00000644611.1:c.325G>A	ENSP00000495423.1:p.Gly109Arg
ENST00000272286.2:c.313G>A	ENSP00000272286.2:p.Gly105Arg
NM_022437.2:c.313G>A	NP_071882.1:p.Gly105Arg
XM_005264483.2:c.313G>A	XP_005264540.1:p.Gly105Arg
XM_011533029.1:c.325G>A	XP_011531331.1:p.Gly109Arg
XM_011533030.1:c.325G>A	XP_011531332.1:p.Gly109Arg
XM_011533031.1:c.97G>A	XP_011531333.1:p.Gly33Arg
XR_939707.1:n.815G>A
NM_001357321.1:c.313G>A	NP_001344250.1:p.Gly105Arg
XM_011533029.2:c.325G>A	XP_011531331.1:p.Gly109Arg
XM_011533030.2:c.325G>A	XP_011531332.1:p.Gly109Arg
XR_001738891.1:n.829G>A
XR_939707.2:n.829G>A
NM_022437.3:c.313G>A MANE Select	NP_071882.1:p.Gly105Arg
NM_001357321.2:c.313G>A	NP_001344250.1:p.Gly105Arg