Canonical Allele Identifier: CA2493964835

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877269G= , CM000664.2:g.43877269G=	GRCh38
NC_000002.11:g.44104408G= , CM000664.1:g.44104408G=	GRCh37
NC_000002.10:g.43957912G=	NCBI36
NG_008884.1:g.43306G=
NG_008884.2:g.50328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1757-292G= MANE Select	ENSP00000272286.2:n.1757-292G=
ENST00000272286.2:c.1757-292G=	ENSP00000272286.2:n.1757-292G=
NM_022437.2:c.1757-292G=	NP_071882.1:n.1757-292G=
XM_005264483.2:c.1754-292G=	XP_005264540.1:n.1754-292G=
XM_011533029.1:c.1769-292G=	XP_011531331.1:n.1769-292G=
XM_011533030.1:c.1766-292G=	XP_011531332.1:n.1766-292G=
XM_011533031.1:c.1541-292G=	XP_011531333.1:n.1541-292G=
XR_939707.1:n.2259-292G=
NM_001357321.1:c.1754-292G=	NP_001344250.1:n.1754-292G=
XM_011533029.2:c.1769-292G=	XP_011531331.1:n.1769-292G=
XM_011533030.2:c.1766-292G=	XP_011531332.1:n.1766-292G=
XR_001738891.1:n.2273-292G=
XR_939707.2:n.2273-292G=
NM_022437.3:c.1757-292G= MANE Select	NP_071882.1:n.1757-292G=
NM_001357321.2:c.1754-292G=	NP_001344250.1:n.1754-292G=