Canonical Allele Identifier: CA346663681
Gene: ABCG8 HGNC NCBI

Linked Data

gnomAD v4: 2-43846294-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43846294C>T , CM000664.2:g.43846294C>T GRCh38
NC_000002.11:g.44073433C>T , CM000664.1:g.44073433C>T GRCh37
NC_000002.10:g.43926937C>T NCBI36
NG_008884.1:g.12331C>T
NG_008884.2:g.19353C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.305C>T MANE Select ENSP00000272286.2:p.Ala102Val
ENST00000643284.1:n.762C>T
ENST00000644611.1:c.317C>T ENSP00000495423.1:p.Ala106Val
ENST00000272286.2:c.305C>T ENSP00000272286.2:p.Ala102Val
NM_022437.2:c.305C>T NP_071882.1:p.Ala102Val
XM_005264483.2:c.305C>T XP_005264540.1:p.Ala102Val
XM_011533029.1:c.317C>T XP_011531331.1:p.Ala106Val
XM_011533030.1:c.317C>T XP_011531332.1:p.Ala106Val
XM_011533031.1:c.89C>T XP_011531333.1:p.Ala30Val
XR_939707.1:n.807C>T
NM_001357321.1:c.305C>T NP_001344250.1:p.Ala102Val
XM_011533029.2:c.317C>T XP_011531331.1:p.Ala106Val
XM_011533030.2:c.317C>T XP_011531332.1:p.Ala106Val
XR_001738891.1:n.821C>T
XR_939707.2:n.821C>T
NM_022437.3:c.305C>T MANE Select NP_071882.1:p.Ala102Val
NM_001357321.2:c.305C>T NP_001344250.1:p.Ala102Val