Canonical Allele Identifier: CA46475029

Gene: ABCG8

Linked Data

• dbSNP Id: rs573740275
• gnomAD v2: 2-44105123-C-T
• gnomAD v3: 2-43877984-C-T
• gnomAD v4: 2-43877984-C-T
• MyVariant Identifiers: chr2:g.44105123C>T (hg19) ; chr2:g.43877984C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877984C>T , CM000664.2:g.43877984C>T	GRCh38
NC_000002.11:g.44105123C>T , CM000664.1:g.44105123C>T	GRCh37
NC_000002.10:g.43958627C>T	NCBI36
NG_008884.1:g.44021C>T
NG_008884.2:g.51043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*71C>T MANE Select	ENSP00000272286.2:n.*71C>T
ENST00000272286.2:c.*71C>T	ENSP00000272286.2:n.*71C>T
NM_022437.2:c.*71C>T	NP_071882.1:n.*71C>T
XM_005264483.2:c.*71C>T	XP_005264540.1:n.*71C>T
XM_011533029.1:c.*71C>T	XP_011531331.1:n.*71C>T
XM_011533030.1:c.*71C>T	XP_011531332.1:n.*71C>T
XM_011533031.1:c.*71C>T	XP_011531333.1:n.*71C>T
XR_939707.1:n.2595C>T
NM_001357321.1:c.*71C>T	NP_001344250.1:n.*71C>T
XM_011533029.2:c.*71C>T	XP_011531331.1:n.*71C>T
XM_011533030.2:c.*71C>T	XP_011531332.1:n.*71C>T
XR_001738891.1:n.2609C>T
XR_939707.2:n.2609C>T
NM_022437.3:c.*71C>T MANE Select	NP_071882.1:n.*71C>T
NM_001357321.2:c.*71C>T	NP_001344250.1:n.*71C>T