Canonical Allele Identifier: CA346670496

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102432G>C (hg19) ; chr2:g.43875293G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875293G>C , CM000664.2:g.43875293G>C	GRCh38
NC_000002.11:g.44102432G>C , CM000664.1:g.44102432G>C	GRCh37
NC_000002.10:g.43955936G>C	NCBI36
NG_008884.1:g.41330G>C
NG_008884.2:g.48352G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1636G>C MANE Select	ENSP00000272286.2:p.Ala546Pro
ENST00000272286.2:c.1636G>C	ENSP00000272286.2:p.Ala546Pro
NM_022437.2:c.1636G>C	NP_071882.1:p.Ala546Pro
XM_005264483.2:c.1633G>C	XP_005264540.1:p.Ala545Pro
XM_011533029.1:c.1648G>C	XP_011531331.1:p.Ala550Pro
XM_011533030.1:c.1645G>C	XP_011531332.1:p.Ala549Pro
XM_011533031.1:c.1420G>C	XP_011531333.1:p.Ala474Pro
XR_939707.1:n.2138G>C
NM_001357321.1:c.1633G>C	NP_001344250.1:p.Ala545Pro
XM_011533029.2:c.1648G>C	XP_011531331.1:p.Ala550Pro
XM_011533030.2:c.1645G>C	XP_011531332.1:p.Ala549Pro
XR_001738891.1:n.2152G>C
XR_939707.2:n.2152G>C
NM_022437.3:c.1636G>C MANE Select	NP_071882.1:p.Ala546Pro
NM_001357321.2:c.1633G>C	NP_001344250.1:p.Ala545Pro