Canonical Allele Identifier: CA1181422662
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1660708821
gnomAD v4: 1-94047117-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047117G>A , CM000663.2:g.94047117G>A GRCh38
NC_000001.10:g.94512673G>A , CM000663.1:g.94512673G>A GRCh37
NC_000001.9:g.94285261G>A NCBI36
NG_009073.1:g.79033C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2744-24C>T MANE Select ENSP00000359245.3:n.2744-24C>T
ENST00000649773.1:c.2522-24C>T ENSP00000496882.1:n.2522-24C>T
ENST00000370225.3:c.2744-24C>T ENSP00000359245.3:n.2744-24C>T
ENST00000536513.5:c.-64-7028C>T ENSP00000439707.2:n.-64-7028C>T
NM_000350.2:c.2744-24C>T NP_000341.2:n.2744-24C>T
NM_000350.3:c.2744-24C>T MANE Select NP_000341.2:n.2744-24C>T