Canonical Allele Identifier: CA425908142

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102338C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875199C>A , CM000664.2:g.43875199C>A	GRCh38
NC_000002.11:g.44102338C>A , CM000664.1:g.44102338C>A	GRCh37
NC_000002.10:g.43955842C>A	NCBI36
NG_008884.1:g.41236C>A
NG_008884.2:g.48258C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1542C>A MANE Select	ENSP00000272286.2:p.Pro514=
ENST00000272286.2:c.1542C>A	ENSP00000272286.2:p.Pro514=
NM_022437.2:c.1542C>A	NP_071882.1:p.Pro514=
XM_005264483.2:c.1539C>A	XP_005264540.1:p.Pro513=
XM_011533029.1:c.1554C>A	XP_011531331.1:p.Pro518=
XM_011533030.1:c.1551C>A	XP_011531332.1:p.Pro517=
XM_011533031.1:c.1326C>A	XP_011531333.1:p.Pro442=
XR_939707.1:n.2044C>A
NM_001357321.1:c.1539C>A	NP_001344250.1:p.Pro513=
XM_011533029.2:c.1554C>A	XP_011531331.1:p.Pro518=
XM_011533030.2:c.1551C>A	XP_011531332.1:p.Pro517=
XR_001738891.1:n.2058C>A
XR_939707.2:n.2058C>A
NM_022437.3:c.1542C>A MANE Select	NP_071882.1:p.Pro514=
NM_001357321.2:c.1539C>A	NP_001344250.1:p.Pro513=