Canonical Allele Identifier: CA418806809
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-93996120-G-T
MyVariant Identifiers: chr1:g.94461676G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93996120G>T , CM000663.2:g.93996120G>T GRCh38
NC_000001.10:g.94461676G>T , CM000663.1:g.94461676G>T GRCh37
NC_000001.9:g.94234264G>T NCBI36
NG_009073.1:g.130030C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6805C>A MANE Select ENSP00000359245.3:p.Arg2269=
ENST00000370225.3:c.6805C>A ENSP00000359245.3:p.Arg2269=
ENST00000536513.5:c.3181C>A ENSP00000439707.2:p.Arg1061=
NM_000350.2:c.6805C>A NP_000341.2:p.Arg2269=
NM_000350.3:c.6805C>A MANE Select NP_000341.2:p.Arg2269=
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Search 100 bp 3'