Canonical Allele Identifier: CA418811984
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2830942
ClinVar RCV Id: RCV003678911
dbSNP Id: rs1801359

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001891G>T , CM000663.2:g.94001891G>T GRCh38
NC_000001.10:g.94467447G>T , CM000663.1:g.94467447G>T GRCh37
NC_000001.9:g.94240035G>T NCBI36
NG_009073.1:g.124259C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6249C>A MANE Select ENSP00000359245.3:p.Ile2083=
ENST00000370225.3:c.6249C>A ENSP00000359245.3:p.Ile2083=
ENST00000465352.1:n.665C>A
ENST00000536513.5:c.2625C>A ENSP00000439707.2:p.Ile875=
NM_000350.2:c.6249C>A NP_000341.2:p.Ile2083=
NM_000350.3:c.6249C>A MANE Select NP_000341.2:p.Ile2083=