Canonical Allele Identifier: CA2493963685

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875318C= , CM000664.2:g.43875318C=	GRCh38
NC_000002.11:g.44102457C= , CM000664.1:g.44102457C=	GRCh37
NC_000002.10:g.43955961C=	NCBI36
NG_008884.1:g.41355C=
NG_008884.2:g.48377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1661C= MANE Select	ENSP00000272286.2:p.Pro554=
ENST00000272286.2:c.1661C=	ENSP00000272286.2:p.Pro554=
NM_022437.2:c.1661C=	NP_071882.1:p.Pro554=
XM_005264483.2:c.1658C=	XP_005264540.1:p.Pro553=
XM_011533029.1:c.1673C=	XP_011531331.1:p.Pro558=
XM_011533030.1:c.1670C=	XP_011531332.1:p.Pro557=
XM_011533031.1:c.1445C=	XP_011531333.1:p.Pro482=
XR_939707.1:n.2163C=
NM_001357321.1:c.1658C=	NP_001344250.1:p.Pro553=
XM_011533029.2:c.1673C=	XP_011531331.1:p.Pro558=
XM_011533030.2:c.1670C=	XP_011531332.1:p.Pro557=
XR_001738891.1:n.2177C=
XR_939707.2:n.2177C=
NM_022437.3:c.1661C= MANE Select	NP_071882.1:p.Pro554=
NM_001357321.2:c.1658C=	NP_001344250.1:p.Pro553=