Canonical Allele Identifier: CA2658828142

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43846422-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846422C>A , CM000664.2:g.43846422C>A	GRCh38
NC_000002.11:g.44073561C>A , CM000664.1:g.44073561C>A	GRCh37
NC_000002.10:g.43927065C>A	NCBI36
NG_008884.1:g.12459C>A
NG_008884.2:g.19481C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.322+111C>A MANE Select	ENSP00000272286.2:n.322+111C>A
ENST00000643284.1:n.890C>A
ENST00000644611.1:c.334+111C>A	ENSP00000495423.1:n.334+111C>A
ENST00000272286.2:c.322+111C>A	ENSP00000272286.2:n.322+111C>A
NM_022437.2:c.322+111C>A	NP_071882.1:n.322+111C>A
XM_005264483.2:c.322+111C>A	XP_005264540.1:n.322+111C>A
XM_011533029.1:c.334+111C>A	XP_011531331.1:n.334+111C>A
XM_011533030.1:c.334+111C>A	XP_011531332.1:n.334+111C>A
XM_011533031.1:c.106+111C>A	XP_011531333.1:n.106+111C>A
XR_939707.1:n.824+111C>A
NM_001357321.1:c.322+111C>A	NP_001344250.1:n.322+111C>A
XM_011533029.2:c.334+111C>A	XP_011531331.1:n.334+111C>A
XM_011533030.2:c.334+111C>A	XP_011531332.1:n.334+111C>A
XR_001738891.1:n.838+111C>A
XR_939707.2:n.838+111C>A
NM_022437.3:c.322+111C>A MANE Select	NP_071882.1:n.322+111C>A
NM_001357321.2:c.322+111C>A	NP_001344250.1:n.322+111C>A