Canonical Allele Identifier: CA957498
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390241
ClinVar RCV Id: RCV001890900
dbSNP Id: rs779572379
ExAC: 1:94487449 G / A
gnomAD v2: 1-94487449-G-A
gnomAD v3: 1-94021893-G-A
gnomAD v4: 1-94021893-G-A
MyVariant Identifiers: chr1:g.94487449G>A (hg19) chr1:g.94021893G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021893G>A , CM000663.2:g.94021893G>A GRCh38
NC_000001.10:g.94487449G>A , CM000663.1:g.94487449G>A GRCh37
NC_000001.9:g.94260037G>A NCBI36
NG_009073.1:g.104257C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4726C>T MANE Select ENSP00000359245.3:p.Leu1576Phe
ENST00000370225.3:c.4726C>T ENSP00000359245.3:p.Leu1576Phe
ENST00000460514.1:n.220C>T
ENST00000536513.5:c.1102C>T ENSP00000439707.2:p.Leu368Phe
NM_000350.2:c.4726C>T NP_000341.2:p.Leu1576Phe
NM_000350.3:c.4726C>T MANE Select NP_000341.2:p.Leu1576Phe
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