Canonical Allele Identifier: CA26863696
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs542080932

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041332A>G , CM000663.2:g.94041332A>G GRCh38
NC_000001.10:g.94506888A>G , CM000663.1:g.94506888A>G GRCh37
NC_000001.9:g.94279476A>G NCBI36
NG_009073.1:g.84818T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3399T>C MANE Select ENSP00000359245.3:p.Ile1133=
ENST00000370225.3:c.3399T>C ENSP00000359245.3:p.Ile1133=
ENST00000536513.5:c.-64-1243T>C ENSP00000439707.2:n.-64-1243T>C
NM_000350.2:c.3399T>C NP_000341.2:p.Ile1133=
NM_000350.3:c.3399T>C MANE Select NP_000341.2:p.Ile1133=