Canonical Allele Identifier: CA2493965007

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877575T= , CM000664.2:g.43877575T=	GRCh38
NC_000002.11:g.44104714T= , CM000664.1:g.44104714T=	GRCh37
NC_000002.10:g.43958218T=	NCBI36
NG_008884.1:g.43612T=
NG_008884.2:g.50634T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1771T= MANE Select	ENSP00000272286.2:p.Ser591=
ENST00000272286.2:c.1771T=	ENSP00000272286.2:p.Ser591=
NM_022437.2:c.1771T=	NP_071882.1:p.Ser591=
XM_005264483.2:c.1768T=	XP_005264540.1:p.Ser590=
XM_011533029.1:c.1783T=	XP_011531331.1:p.Ser595=
XM_011533030.1:c.1780T=	XP_011531332.1:p.Ser594=
XM_011533031.1:c.1555T=	XP_011531333.1:p.Ser519=
XR_939707.1:n.2273T=
NM_001357321.1:c.1768T=	NP_001344250.1:p.Ser590=
XM_011533029.2:c.1783T=	XP_011531331.1:p.Ser595=
XM_011533030.2:c.1780T=	XP_011531332.1:p.Ser594=
XR_001738891.1:n.2287T=
XR_939707.2:n.2287T=
NM_022437.3:c.1771T= MANE Select	NP_071882.1:p.Ser591=
NM_001357321.2:c.1768T=	NP_001344250.1:p.Ser590=