Canonical Allele Identifier: CA26843973
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs927586489
gnomAD v4: 1-94056523-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056523C>A , CM000663.2:g.94056523C>A GRCh38
NC_000001.10:g.94522079C>A , CM000663.1:g.94522079C>A GRCh37
NC_000001.9:g.94294667C>A NCBI36
NG_009073.1:g.69627G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2382+78G>T MANE Select ENSP00000359245.3:n.2382+78G>T
ENST00000649773.1:c.2161-1208G>T ENSP00000496882.1:n.2161-1208G>T
ENST00000370225.3:c.2382+78G>T ENSP00000359245.3:n.2382+78G>T
ENST00000536513.5:c.-65+6651G>T ENSP00000439707.2:n.-65+6651G>T
NM_000350.2:c.2382+78G>T NP_000341.2:n.2382+78G>T
NM_000350.3:c.2382+78G>T MANE Select NP_000341.2:n.2382+78G>T