Canonical Allele Identifier: CA2493965128

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877785G= , CM000664.2:g.43877785G=	GRCh38
NC_000002.11:g.44104924G= , CM000664.1:g.44104924G=	GRCh37
NC_000002.10:g.43958428G=	NCBI36
NG_008884.1:g.43822G=
NG_008884.2:g.50844G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1894G= MANE Select	ENSP00000272286.2:p.Val632=
ENST00000272286.2:c.1894G=	ENSP00000272286.2:p.Val632=
NM_022437.2:c.1894G=	NP_071882.1:p.Val632=
XM_005264483.2:c.1891G=	XP_005264540.1:p.Val631=
XM_011533029.1:c.1906G=	XP_011531331.1:p.Val636=
XM_011533030.1:c.1903G=	XP_011531332.1:p.Val635=
XM_011533031.1:c.1678G=	XP_011531333.1:p.Val560=
XR_939707.1:n.2396G=
NM_001357321.1:c.1891G=	NP_001344250.1:p.Val631=
XM_011533029.2:c.1906G=	XP_011531331.1:p.Val636=
XM_011533030.2:c.1903G=	XP_011531332.1:p.Val635=
XR_001738891.1:n.2410G=
XR_939707.2:n.2410G=
NM_022437.3:c.1894G= MANE Select	NP_071882.1:p.Val632=
NM_001357321.2:c.1891G=	NP_001344250.1:p.Val631=