Canonical Allele Identifier: CA46475256

Gene: ABCG8

Linked Data

• dbSNP Id: rs902595685
• gnomAD v3: 2-43878186-C-T
• gnomAD v4: 2-43878186-C-T
• MyVariant Identifiers: chr2:g.44105325C>T (hg19) ; chr2:g.43878186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43878186C>T , CM000664.2:g.43878186C>T	GRCh38
NC_000002.11:g.44105325C>T , CM000664.1:g.44105325C>T	GRCh37
NC_000002.10:g.43958829C>T	NCBI36
NG_008884.1:g.44223C>T
NG_008884.2:g.51245C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*273C>T MANE Select	ENSP00000272286.2:n.*273C>T
ENST00000272286.2:c.*273C>T	ENSP00000272286.2:n.*273C>T
NM_022437.2:c.*273C>T	NP_071882.1:n.*273C>T
XM_005264483.2:c.*273C>T	XP_005264540.1:n.*273C>T
XM_011533029.1:c.*273C>T	XP_011531331.1:n.*273C>T
XM_011533030.1:c.*273C>T	XP_011531332.1:n.*273C>T
XM_011533031.1:c.*273C>T	XP_011531333.1:n.*273C>T
XR_939707.1:n.2797C>T
NM_001357321.1:c.*273C>T	NP_001344250.1:n.*273C>T
XM_011533029.2:c.*273C>T	XP_011531331.1:n.*273C>T
XM_011533030.2:c.*273C>T	XP_011531332.1:n.*273C>T
XR_001738891.1:n.2811C>T
XR_939707.2:n.2811C>T
NM_022437.3:c.*273C>T MANE Select	NP_071882.1:n.*273C>T
NM_001357321.2:c.*273C>T	NP_001344250.1:n.*273C>T