Canonical Allele Identifier: CA2493965152

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877830G= , CM000664.2:g.43877830G=	GRCh38
NC_000002.11:g.44104969G= , CM000664.1:g.44104969G=	GRCh37
NC_000002.10:g.43958473G=	NCBI36
NG_008884.1:g.43867G=
NG_008884.2:g.50889G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1939G= MANE Select	ENSP00000272286.2:p.Val647=
ENST00000272286.2:c.1939G=	ENSP00000272286.2:p.Val647=
NM_022437.2:c.1939G=	NP_071882.1:p.Val647=
XM_005264483.2:c.1936G=	XP_005264540.1:p.Val646=
XM_011533029.1:c.1951G=	XP_011531331.1:p.Val651=
XM_011533030.1:c.1948G=	XP_011531332.1:p.Val650=
XM_011533031.1:c.1723G=	XP_011531333.1:p.Val575=
XR_939707.1:n.2441G=
NM_001357321.1:c.1936G=	NP_001344250.1:p.Val646=
XM_011533029.2:c.1951G=	XP_011531331.1:p.Val651=
XM_011533030.2:c.1948G=	XP_011531332.1:p.Val650=
XR_001738891.1:n.2455G=
XR_939707.2:n.2455G=
NM_022437.3:c.1939G= MANE Select	NP_071882.1:p.Val647=
NM_001357321.2:c.1936G=	NP_001344250.1:p.Val646=