Canonical Allele Identifier: CA2493961758

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43871997G= , CM000664.2:g.43871997G=	GRCh38
NC_000002.11:g.44099136G= , CM000664.1:g.44099136G=	GRCh37
NC_000002.10:g.43952640G=	NCBI36
NG_008884.1:g.38034G=
NG_008884.2:g.45056G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.986G= MANE Select	ENSP00000272286.2:p.Arg329=
ENST00000644611.1:c.998G=	ENSP00000495423.1:p.Arg333=
ENST00000272286.2:c.986G=	ENSP00000272286.2:p.Arg329=
NM_022437.2:c.986G=	NP_071882.1:p.Arg329=
XM_005264483.2:c.986G=	XP_005264540.1:p.Arg329=
XM_011533029.1:c.998G=	XP_011531331.1:p.Arg333=
XM_011533030.1:c.998G=	XP_011531332.1:p.Arg333=
XM_011533031.1:c.770G=	XP_011531333.1:p.Arg257=
XR_939707.1:n.1488G=
NM_001357321.1:c.986G=	NP_001344250.1:p.Arg329=
XM_011533029.2:c.998G=	XP_011531331.1:p.Arg333=
XM_011533030.2:c.998G=	XP_011531332.1:p.Arg333=
XR_001738891.1:n.1502G=
XR_939707.2:n.1502G=
NM_022437.3:c.986G= MANE Select	NP_071882.1:p.Arg329=
NM_001357321.2:c.986G=	NP_001344250.1:p.Arg329=