Canonical Allele Identifier: CA769083359

Gene: ABCG8

Linked Data

• dbSNP Id: rs1200534768
• MyVariant Identifiers: chr2:g.44105255T>A (hg19) ; chr2:g.43878116T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43878116T>A , CM000664.2:g.43878116T>A	GRCh38
NC_000002.11:g.44105255T>A , CM000664.1:g.44105255T>A	GRCh37
NC_000002.10:g.43958759T>A	NCBI36
NG_008884.1:g.44153T>A
NG_008884.2:g.51175T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*203T>A MANE Select	ENSP00000272286.2:n.*203T>A
ENST00000272286.2:c.*203T>A	ENSP00000272286.2:n.*203T>A
NM_022437.2:c.*203T>A	NP_071882.1:n.*203T>A
XM_005264483.2:c.*203T>A	XP_005264540.1:n.*203T>A
XM_011533029.1:c.*203T>A	XP_011531331.1:n.*203T>A
XM_011533030.1:c.*203T>A	XP_011531332.1:n.*203T>A
XM_011533031.1:c.*203T>A	XP_011531333.1:n.*203T>A
XR_939707.1:n.2727T>A
NM_001357321.1:c.*203T>A	NP_001344250.1:n.*203T>A
XM_011533029.2:c.*203T>A	XP_011531331.1:n.*203T>A
XM_011533030.2:c.*203T>A	XP_011531332.1:n.*203T>A
XR_001738891.1:n.2741T>A
XR_939707.2:n.2741T>A
NM_022437.3:c.*203T>A MANE Select	NP_071882.1:n.*203T>A
NM_001357321.2:c.*203T>A	NP_001344250.1:n.*203T>A