Canonical Allele Identifier: CA2493945411

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846759C= , CM000664.2:g.43846759C=	GRCh38
NC_000002.11:g.44073898C= , CM000664.1:g.44073898C=	GRCh37
NC_000002.10:g.43927402C=	NCBI36
NG_008884.1:g.12796C=
NG_008884.2:g.19818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.322+448C= MANE Select	ENSP00000272286.2:n.322+448C=
ENST00000643284.1:n.1227C=
ENST00000644611.1:c.334+448C=	ENSP00000495423.1:n.334+448C=
ENST00000272286.2:c.322+448C=	ENSP00000272286.2:n.322+448C=
NM_022437.2:c.322+448C=	NP_071882.1:n.322+448C=
XM_005264483.2:c.322+448C=	XP_005264540.1:n.322+448C=
XM_011533029.1:c.334+448C=	XP_011531331.1:n.334+448C=
XM_011533030.1:c.334+448C=	XP_011531332.1:n.334+448C=
XM_011533031.1:c.106+448C=	XP_011531333.1:n.106+448C=
XR_939707.1:n.824+448C=
NM_001357321.1:c.322+448C=	NP_001344250.1:n.322+448C=
XM_011533029.2:c.334+448C=	XP_011531331.1:n.334+448C=
XM_011533030.2:c.334+448C=	XP_011531332.1:n.334+448C=
XR_001738891.1:n.838+448C=
XR_939707.2:n.838+448C=
NM_022437.3:c.322+448C= MANE Select	NP_071882.1:n.322+448C=
NM_001357321.2:c.322+448C=	NP_001344250.1:n.322+448C=