Canonical Allele Identifier: CA2493963585

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875147T= , CM000664.2:g.43875147T=	GRCh38
NC_000002.11:g.44102286T= , CM000664.1:g.44102286T=	GRCh37
NC_000002.10:g.43955790T=	NCBI36
NG_008884.1:g.41184T=
NG_008884.2:g.48206T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1490T= MANE Select	ENSP00000272286.2:p.Ile497=
ENST00000272286.2:c.1490T=	ENSP00000272286.2:p.Ile497=
NM_022437.2:c.1490T=	NP_071882.1:p.Ile497=
XM_005264483.2:c.1487T=	XP_005264540.1:p.Ile496=
XM_011533029.1:c.1502T=	XP_011531331.1:p.Ile501=
XM_011533030.1:c.1499T=	XP_011531332.1:p.Ile500=
XM_011533031.1:c.1274T=	XP_011531333.1:p.Ile425=
XR_939707.1:n.1992T=
NM_001357321.1:c.1487T=	NP_001344250.1:p.Ile496=
XM_011533029.2:c.1502T=	XP_011531331.1:p.Ile501=
XM_011533030.2:c.1499T=	XP_011531332.1:p.Ile500=
XR_001738891.1:n.2006T=
XR_939707.2:n.2006T=
NM_022437.3:c.1490T= MANE Select	NP_071882.1:p.Ile497=
NM_001357321.2:c.1487T=	NP_001344250.1:p.Ile496=