Canonical Allele Identifier: CA341276817
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs61749438
gnomAD v2: 1-94520689-C-A
gnomAD v4: 1-94055133-C-A
MyVariant Identifiers: chr1:g.94520689C>A (hg19) chr1:g.94055133C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94055133C>A , CM000663.2:g.94055133C>A GRCh38
NC_000001.10:g.94520689C>A , CM000663.1:g.94520689C>A GRCh37
NC_000001.9:g.94293277C>A NCBI36
NG_009073.1:g.71017G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.2565G>T MANE Select ENSP00000359245.3:p.Trp855Cys
ENST00000649773.1:c.2343G>T ENSP00000496882.1:p.Trp781Cys
ENST00000370225.3:c.2565G>T ENSP00000359245.3:p.Trp855Cys
ENST00000536513.5:c.-65+8041G>T ENSP00000439707.2:n.-65+8041G>T
NM_000350.2:c.2565G>T NP_000341.2:p.Trp855Cys
NM_000350.3:c.2565G>T MANE Select NP_000341.2:p.Trp855Cys
Search 100 bp 5'
Search 100 bp 3'