Canonical Allele Identifier: CA958127
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs761945060
ExAC: 1:94512514 G / A
gnomAD v2: 1-94512514-G-A
gnomAD v4: 1-94046958-G-A
MyVariant Identifiers: chr1:g.94512514G>A (hg19) chr1:g.94046958G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046958G>A , CM000663.2:g.94046958G>A GRCh38
NC_000001.10:g.94512514G>A , CM000663.1:g.94512514G>A GRCh37
NC_000001.9:g.94285102G>A NCBI36
NG_009073.1:g.79192C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.2879C>T MANE Select ENSP00000359245.3:p.Ala960Val
ENST00000649773.1:c.2657C>T ENSP00000496882.1:p.Ala886Val
ENST00000370225.3:c.2879C>T ENSP00000359245.3:p.Ala960Val
ENST00000536513.5:c.-64-6869C>T ENSP00000439707.2:n.-64-6869C>T
NM_000350.2:c.2879C>T NP_000341.2:p.Ala960Val
NM_000350.3:c.2879C>T MANE Select NP_000341.2:p.Ala960Val
Search 100 bp 5'
Search 100 bp 3'