Canonical Allele Identifier: CA26846621
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 681135
ClinVar RCV Id: RCV000840981 RCV004538155
dbSNP Id: rs976467572
gnomAD v2: 1-94526291-A-G
gnomAD v3: 1-94060735-A-G
gnomAD v4: 1-94060735-A-G
MyVariant Identifiers: chr1:g.94526291A>G (hg19) chr1:g.94060735A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060735A>G , CM000663.2:g.94060735A>G GRCh38
NC_000001.10:g.94526291A>G , CM000663.1:g.94526291A>G GRCh37
NC_000001.9:g.94298879A>G NCBI36
NG_009073.1:g.65415T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1962T>C MANE Select ENSP00000359245.3:p.Cys654=
ENST00000649773.1:c.1962T>C ENSP00000496882.1:p.Cys654=
ENST00000370225.3:c.1962T>C ENSP00000359245.3:p.Cys654=
ENST00000472033.1:n.82T>C
ENST00000536513.5:c.-65+2439T>C ENSP00000439707.2:n.-65+2439T>C
NM_000350.2:c.1962T>C NP_000341.2:p.Cys654=
NM_000350.3:c.1962T>C MANE Select NP_000341.2:p.Cys654=
Search 100 bp 5'
Search 100 bp 3'