Canonical Allele Identifier: CA957656
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 513579
ClinVar RCV Id: RCV000616045 RCV001447889
dbSNP Id: rs368147821
ExAC: 1:94496040 G / A
gnomAD v2: 1-94496040-G-A
gnomAD v3: 1-94030484-G-A
gnomAD v4: 1-94030484-G-A
MyVariant Identifiers: chr1:g.94496040G>A (hg19) chr1:g.94030484G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030484G>A , CM000663.2:g.94030484G>A GRCh38
NC_000001.10:g.94496040G>A , CM000663.1:g.94496040G>A GRCh37
NC_000001.9:g.94268628G>A NCBI36
NG_009073.1:g.95666C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4296C>T MANE Select ENSP00000359245.3:p.Asp1432=
ENST00000370225.3:c.4296C>T ENSP00000359245.3:p.Asp1432=
ENST00000536513.5:c.672C>T ENSP00000439707.2:p.Asp224=
NM_000350.2:c.4296C>T NP_000341.2:p.Asp1432=
NM_000350.3:c.4296C>T MANE Select NP_000341.2:p.Asp1432=
Search 100 bp 5'
Search 100 bp 3'