Canonical Allele Identifier: CA418808285
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2707819
ClinVar RCV Id: RCV003545047
MyVariant Identifiers: chr1:g.94463465G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997909G>A , CM000663.2:g.93997909G>A GRCh38
NC_000001.10:g.94463465G>A , CM000663.1:g.94463465G>A GRCh37
NC_000001.9:g.94236053G>A NCBI36
NG_009073.1:g.128241C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6681C>T MANE Select ENSP00000359245.3:p.Asp2227=
ENST00000370225.3:c.6681C>T ENSP00000359245.3:p.Asp2227=
ENST00000536513.5:c.3057C>T ENSP00000439707.2:p.Asp1019=
NM_000350.2:c.6681C>T NP_000341.2:p.Asp2227=
NM_000350.3:c.6681C>T MANE Select NP_000341.2:p.Asp2227=
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