Canonical Allele Identifier: CA346663592

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43846256-G-C
• MyVariant Identifiers: chr2:g.44073395G>C (hg19) ; chr2:g.43846256G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846256G>C , CM000664.2:g.43846256G>C	GRCh38
NC_000002.11:g.44073395G>C , CM000664.1:g.44073395G>C	GRCh37
NC_000002.10:g.43926899G>C	NCBI36
NG_008884.1:g.12293G>C
NG_008884.2:g.19315G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.267G>C MANE Select	ENSP00000272286.2:p.Gln89His
ENST00000643284.1:n.724G>C
ENST00000644611.1:c.279G>C	ENSP00000495423.1:p.Gln93His
ENST00000272286.2:c.267G>C	ENSP00000272286.2:p.Gln89His
NM_022437.2:c.267G>C	NP_071882.1:p.Gln89His
XM_005264483.2:c.267G>C	XP_005264540.1:p.Gln89His
XM_011533029.1:c.279G>C	XP_011531331.1:p.Gln93His
XM_011533030.1:c.279G>C	XP_011531332.1:p.Gln93His
XM_011533031.1:c.51G>C	XP_011531333.1:p.Gln17His
XR_939707.1:n.769G>C
NM_001357321.1:c.267G>C	NP_001344250.1:p.Gln89His
XM_011533029.2:c.279G>C	XP_011531331.1:p.Gln93His
XM_011533030.2:c.279G>C	XP_011531332.1:p.Gln93His
XR_001738891.1:n.783G>C
XR_939707.2:n.783G>C
NM_022437.3:c.267G>C MANE Select	NP_071882.1:p.Gln89His
NM_001357321.2:c.267G>C	NP_001344250.1:p.Gln89His