Canonical Allele Identifier: CA2493965310

Gene: ABCG8

Linked Data

• dbSNP Id: rs1670023668

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43878112T>G , CM000664.2:g.43878112T>G	GRCh38
NC_000002.11:g.44105251T>G , CM000664.1:g.44105251T>G	GRCh37
NC_000002.10:g.43958755T>G	NCBI36
NG_008884.1:g.44149T>G
NG_008884.2:g.51171T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*199T>G MANE Select	ENSP00000272286.2:n.*199T>G
ENST00000272286.2:c.*199T>G	ENSP00000272286.2:n.*199T>G
NM_022437.2:c.*199T>G	NP_071882.1:n.*199T>G
XM_005264483.2:c.*199T>G	XP_005264540.1:n.*199T>G
XM_011533029.1:c.*199T>G	XP_011531331.1:n.*199T>G
XM_011533030.1:c.*199T>G	XP_011531332.1:n.*199T>G
XM_011533031.1:c.*199T>G	XP_011531333.1:n.*199T>G
XR_939707.1:n.2723T>G
NM_001357321.1:c.*199T>G	NP_001344250.1:n.*199T>G
XM_011533029.2:c.*199T>G	XP_011531331.1:n.*199T>G
XM_011533030.2:c.*199T>G	XP_011531332.1:n.*199T>G
XR_001738891.1:n.2737T>G
XR_939707.2:n.2737T>G
NM_022437.3:c.*199T>G MANE Select	NP_071882.1:n.*199T>G
NM_001357321.2:c.*199T>G	NP_001344250.1:n.*199T>G