Canonical Allele Identifier: CA418808521
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1608126
ClinVar RCV Id: RCV002145102
dbSNP Id: rs1299747532
gnomAD v3: 1-93997966-G-A
gnomAD v4: 1-93997966-G-A
MyVariant Identifiers: chr1:g.94463522G>A (hg19) chr1:g.93997966G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997966G>A , CM000663.2:g.93997966G>A GRCh38
NC_000001.10:g.94463522G>A , CM000663.1:g.94463522G>A GRCh37
NC_000001.9:g.94236110G>A NCBI36
NG_009073.1:g.128184C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6624C>T MANE Select ENSP00000359245.3:p.Phe2208=
ENST00000370225.3:c.6624C>T ENSP00000359245.3:p.Phe2208=
ENST00000536513.5:c.3000C>T ENSP00000439707.2:p.Phe1000=
NM_000350.2:c.6624C>T NP_000341.2:p.Phe2208=
NM_000350.3:c.6624C>T MANE Select NP_000341.2:p.Phe2208=
Search 100 bp 5'
Search 100 bp 3'