Canonical Allele Identifier: CA2658828389

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43846706-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846706C>A , CM000664.2:g.43846706C>A	GRCh38
NC_000002.11:g.44073845C>A , CM000664.1:g.44073845C>A	GRCh37
NC_000002.10:g.43927349C>A	NCBI36
NG_008884.1:g.12743C>A
NG_008884.2:g.19765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.322+395C>A MANE Select	ENSP00000272286.2:n.322+395C>A
ENST00000643284.1:n.1174C>A
ENST00000644611.1:c.334+395C>A	ENSP00000495423.1:n.334+395C>A
ENST00000272286.2:c.322+395C>A	ENSP00000272286.2:n.322+395C>A
NM_022437.2:c.322+395C>A	NP_071882.1:n.322+395C>A
XM_005264483.2:c.322+395C>A	XP_005264540.1:n.322+395C>A
XM_011533029.1:c.334+395C>A	XP_011531331.1:n.334+395C>A
XM_011533030.1:c.334+395C>A	XP_011531332.1:n.334+395C>A
XM_011533031.1:c.106+395C>A	XP_011531333.1:n.106+395C>A
XR_939707.1:n.824+395C>A
NM_001357321.1:c.322+395C>A	NP_001344250.1:n.322+395C>A
XM_011533029.2:c.334+395C>A	XP_011531331.1:n.334+395C>A
XM_011533030.2:c.334+395C>A	XP_011531332.1:n.334+395C>A
XR_001738891.1:n.838+395C>A
XR_939707.2:n.838+395C>A
NM_022437.3:c.322+395C>A MANE Select	NP_071882.1:n.322+395C>A
NM_001357321.2:c.322+395C>A	NP_001344250.1:n.322+395C>A