Canonical Allele Identifier: CA2493963729

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875378G= , CM000664.2:g.43875378G=	GRCh38
NC_000002.11:g.44102517G= , CM000664.1:g.44102517G=	GRCh37
NC_000002.10:g.43956021G=	NCBI36
NG_008884.1:g.41415G=
NG_008884.2:g.48437G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1721G= MANE Select	ENSP00000272286.2:p.Gly574=
ENST00000272286.2:c.1721G=	ENSP00000272286.2:p.Gly574=
NM_022437.2:c.1721G=	NP_071882.1:p.Gly574=
XM_005264483.2:c.1718G=	XP_005264540.1:p.Gly573=
XM_011533029.1:c.1733G=	XP_011531331.1:p.Gly578=
XM_011533030.1:c.1730G=	XP_011531332.1:p.Gly577=
XM_011533031.1:c.1505G=	XP_011531333.1:p.Gly502=
XR_939707.1:n.2223G=
NM_001357321.1:c.1718G=	NP_001344250.1:p.Gly573=
XM_011533029.2:c.1733G=	XP_011531331.1:p.Gly578=
XM_011533030.2:c.1730G=	XP_011531332.1:p.Gly577=
XR_001738891.1:n.2237G=
XR_939707.2:n.2237G=
NM_022437.3:c.1721G= MANE Select	NP_071882.1:p.Gly574=
NM_001357321.2:c.1718G=	NP_001344250.1:p.Gly573=