Canonical Allele Identifier: CA346671477

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43877866-T-C
• MyVariant Identifiers: chr2:g.44105005T>C (hg19) ; chr2:g.43877866T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877866T>C , CM000664.2:g.43877866T>C	GRCh38
NC_000002.11:g.44105005T>C , CM000664.1:g.44105005T>C	GRCh37
NC_000002.10:g.43958509T>C	NCBI36
NG_008884.1:g.43903T>C
NG_008884.2:g.50925T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1975T>C MANE Select	ENSP00000272286.2:p.Tyr659His
ENST00000272286.2:c.1975T>C	ENSP00000272286.2:p.Tyr659His
NM_022437.2:c.1975T>C	NP_071882.1:p.Tyr659His
XM_005264483.2:c.1972T>C	XP_005264540.1:p.Tyr658His
XM_011533029.1:c.1987T>C	XP_011531331.1:p.Tyr663His
XM_011533030.1:c.1984T>C	XP_011531332.1:p.Tyr662His
XM_011533031.1:c.1759T>C	XP_011531333.1:p.Tyr587His
XR_939707.1:n.2477T>C
NM_001357321.1:c.1972T>C	NP_001344250.1:p.Tyr658His
XM_011533029.2:c.1987T>C	XP_011531331.1:p.Tyr663His
XM_011533030.2:c.1984T>C	XP_011531332.1:p.Tyr662His
XR_001738891.1:n.2491T>C
XR_939707.2:n.2491T>C
NM_022437.3:c.1975T>C MANE Select	NP_071882.1:p.Tyr659His
NM_001357321.2:c.1972T>C	NP_001344250.1:p.Tyr658His