Canonical Allele Identifier: CA418824970
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1322226342
gnomAD v2: 1-94496031-C-A
gnomAD v3: 1-94030475-C-A
gnomAD v4: 1-94030475-C-A
MyVariant Identifiers: chr1:g.94496031C>A (hg19) chr1:g.94030475C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030475C>A , CM000663.2:g.94030475C>A GRCh38
NC_000001.10:g.94496031C>A , CM000663.1:g.94496031C>A GRCh37
NC_000001.9:g.94268619C>A NCBI36
NG_009073.1:g.95675G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4305G>T MANE Select ENSP00000359245.3:p.Leu1435=
ENST00000370225.3:c.4305G>T ENSP00000359245.3:p.Leu1435=
ENST00000536513.5:c.681G>T ENSP00000439707.2:p.Leu227=
NM_000350.2:c.4305G>T NP_000341.2:p.Leu1435=
NM_000350.3:c.4305G>T MANE Select NP_000341.2:p.Leu1435=
Search 100 bp 5'
Search 100 bp 3'