Canonical Allele Identifier: CA1637079

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43852371G>A , CM000664.2:g.43852371G>A	GRCh38
NC_000002.11:g.44079510G>A , CM000664.1:g.44079510G>A	GRCh37
NC_000002.10:g.43933014G>A	NCBI36
NG_008884.1:g.18408G>A
NG_008884.2:g.25430G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.579G>A MANE Select	NP_071882.1:p.Ala193=
ENST00000272286.4:c.579G>A MANE Select	ENSP00000272286.2:p.Ala193=
NM_001357321.1:c.579G>A	NP_001344250.1:p.Ala193=
NM_001357321.2:c.579G>A	NP_001344250.1:p.Ala193=
NM_022437.2:c.579G>A	NP_071882.1:p.Ala193=
ENST00000272286.2:c.579G>A	ENSP00000272286.2:p.Ala193=
ENST00000644611.1:c.591G>A	ENSP00000495423.1:p.Ala197=
XM_005264483.2:c.579G>A	XP_005264540.1:p.Ala193=
XM_011533029.1:c.591G>A	XP_011531331.1:p.Ala197=
XM_011533029.2:c.591G>A	XP_011531331.1:p.Ala197=
XM_011533030.1:c.591G>A	XP_011531332.1:p.Ala197=
XM_011533030.2:c.591G>A	XP_011531332.1:p.Ala197=
XM_011533031.1:c.363G>A	XP_011531333.1:p.Ala121=
XR_001738891.1:n.1095G>A
XR_939707.1:n.1081G>A
XR_939707.2:n.1095G>A