Canonical Allele Identifier: CA2493963694

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875334C= , CM000664.2:g.43875334C=	GRCh38
NC_000002.11:g.44102473C= , CM000664.1:g.44102473C=	GRCh37
NC_000002.10:g.43955977C=	NCBI36
NG_008884.1:g.41371C=
NG_008884.2:g.48393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1677C= MANE Select	ENSP00000272286.2:p.Ala559=
ENST00000272286.2:c.1677C=	ENSP00000272286.2:p.Ala559=
NM_022437.2:c.1677C=	NP_071882.1:p.Ala559=
XM_005264483.2:c.1674C=	XP_005264540.1:p.Ala558=
XM_011533029.1:c.1689C=	XP_011531331.1:p.Ala563=
XM_011533030.1:c.1686C=	XP_011531332.1:p.Ala562=
XM_011533031.1:c.1461C=	XP_011531333.1:p.Ala487=
XR_939707.1:n.2179C=
NM_001357321.1:c.1674C=	NP_001344250.1:p.Ala558=
XM_011533029.2:c.1689C=	XP_011531331.1:p.Ala563=
XM_011533030.2:c.1686C=	XP_011531332.1:p.Ala562=
XR_001738891.1:n.2193C=
XR_939707.2:n.2193C=
NM_022437.3:c.1677C= MANE Select	NP_071882.1:p.Ala559=
NM_001357321.2:c.1674C=	NP_001344250.1:p.Ala558=