Canonical Allele Identifier: CA2493965172

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877880G= , CM000664.2:g.43877880G=	GRCh38
NC_000002.11:g.44105019G= , CM000664.1:g.44105019G=	GRCh37
NC_000002.10:g.43958523G=	NCBI36
NG_008884.1:g.43917G=
NG_008884.2:g.50939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1989G= MANE Select	ENSP00000272286.2:p.Arg663=
ENST00000272286.2:c.1989G=	ENSP00000272286.2:p.Arg663=
NM_022437.2:c.1989G=	NP_071882.1:p.Arg663=
XM_005264483.2:c.1986G=	XP_005264540.1:p.Arg662=
XM_011533029.1:c.2001G=	XP_011531331.1:p.Arg667=
XM_011533030.1:c.1998G=	XP_011531332.1:p.Arg666=
XM_011533031.1:c.1773G=	XP_011531333.1:p.Arg591=
XR_939707.1:n.2491G=
NM_001357321.1:c.1986G=	NP_001344250.1:p.Arg662=
XM_011533029.2:c.2001G=	XP_011531331.1:p.Arg667=
XM_011533030.2:c.1998G=	XP_011531332.1:p.Arg666=
XR_001738891.1:n.2505G=
XR_939707.2:n.2505G=
NM_022437.3:c.1989G= MANE Select	NP_071882.1:p.Arg663=
NM_001357321.2:c.1986G=	NP_001344250.1:p.Arg662=