Canonical Allele Identifier: CA2493963548

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875092A= , CM000664.2:g.43875092A=	GRCh38
NC_000002.11:g.44102231A= , CM000664.1:g.44102231A=	GRCh37
NC_000002.10:g.43955735A=	NCBI36
NG_008884.1:g.41129A=
NG_008884.2:g.48151A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1489-54A= MANE Select	ENSP00000272286.2:n.1489-54A=
ENST00000272286.2:c.1489-54A=	ENSP00000272286.2:n.1489-54A=
NM_022437.2:c.1489-54A=	NP_071882.1:n.1489-54A=
XM_005264483.2:c.1486-54A=	XP_005264540.1:n.1486-54A=
XM_011533029.1:c.1501-54A=	XP_011531331.1:n.1501-54A=
XM_011533030.1:c.1498-54A=	XP_011531332.1:n.1498-54A=
XM_011533031.1:c.1273-54A=	XP_011531333.1:n.1273-54A=
XR_939707.1:n.1991-54A=
NM_001357321.1:c.1486-54A=	NP_001344250.1:n.1486-54A=
XM_011533029.2:c.1501-54A=	XP_011531331.1:n.1501-54A=
XM_011533030.2:c.1498-54A=	XP_011531332.1:n.1498-54A=
XR_001738891.1:n.2005-54A=
XR_939707.2:n.2005-54A=
NM_022437.3:c.1489-54A= MANE Select	NP_071882.1:n.1489-54A=
NM_001357321.2:c.1486-54A=	NP_001344250.1:n.1486-54A=