Canonical Allele Identifier: CA2493945160

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846283G= , CM000664.2:g.43846283G=	GRCh38
NC_000002.11:g.44073422G= , CM000664.1:g.44073422G=	GRCh37
NC_000002.10:g.43926926G=	NCBI36
NG_008884.1:g.12320G=
NG_008884.2:g.19342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.294G= MANE Select	ENSP00000272286.2:p.Gly98=
ENST00000643284.1:n.751G=
ENST00000644611.1:c.306G=	ENSP00000495423.1:p.Gly102=
ENST00000272286.2:c.294G=	ENSP00000272286.2:p.Gly98=
NM_022437.2:c.294G=	NP_071882.1:p.Gly98=
XM_005264483.2:c.294G=	XP_005264540.1:p.Gly98=
XM_011533029.1:c.306G=	XP_011531331.1:p.Gly102=
XM_011533030.1:c.306G=	XP_011531332.1:p.Gly102=
XM_011533031.1:c.78G=	XP_011531333.1:p.Gly26=
XR_939707.1:n.796G=
NM_001357321.1:c.294G=	NP_001344250.1:p.Gly98=
XM_011533029.2:c.306G=	XP_011531331.1:p.Gly102=
XM_011533030.2:c.306G=	XP_011531332.1:p.Gly102=
XR_001738891.1:n.810G=
XR_939707.2:n.810G=
NM_022437.3:c.294G= MANE Select	NP_071882.1:p.Gly98=
NM_001357321.2:c.294G=	NP_001344250.1:p.Gly98=