Canonical Allele Identifier: CA2493963702

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875345G= , CM000664.2:g.43875345G=	GRCh38
NC_000002.11:g.44102484G= , CM000664.1:g.44102484G=	GRCh37
NC_000002.10:g.43955988G=	NCBI36
NG_008884.1:g.41382G=
NG_008884.2:g.48404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1688G= MANE Select	ENSP00000272286.2:p.Ser563=
ENST00000272286.2:c.1688G=	ENSP00000272286.2:p.Ser563=
NM_022437.2:c.1688G=	NP_071882.1:p.Ser563=
XM_005264483.2:c.1685G=	XP_005264540.1:p.Ser562=
XM_011533029.1:c.1700G=	XP_011531331.1:p.Ser567=
XM_011533030.1:c.1697G=	XP_011531332.1:p.Ser566=
XM_011533031.1:c.1472G=	XP_011531333.1:p.Ser491=
XR_939707.1:n.2190G=
NM_001357321.1:c.1685G=	NP_001344250.1:p.Ser562=
XM_011533029.2:c.1700G=	XP_011531331.1:p.Ser567=
XM_011533030.2:c.1697G=	XP_011531332.1:p.Ser566=
XR_001738891.1:n.2204G=
XR_939707.2:n.2204G=
NM_022437.3:c.1688G= MANE Select	NP_071882.1:p.Ser563=
NM_001357321.2:c.1685G=	NP_001344250.1:p.Ser562=