Canonical Allele Identifier: CA341275588
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94512629G>C (hg19) chr1:g.94047073G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047073G>C , CM000663.2:g.94047073G>C GRCh38
NC_000001.10:g.94512629G>C , CM000663.1:g.94512629G>C GRCh37
NC_000001.9:g.94285217G>C NCBI36
NG_009073.1:g.79077C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2764C>G MANE Select ENSP00000359245.3:p.His922Asp
ENST00000649773.1:c.2542C>G ENSP00000496882.1:p.His848Asp
ENST00000370225.3:c.2764C>G ENSP00000359245.3:p.His922Asp
ENST00000536513.5:c.-64-6984C>G ENSP00000439707.2:n.-64-6984C>G
NM_000350.2:c.2764C>G NP_000341.2:p.His922Asp
NM_000350.3:c.2764C>G MANE Select NP_000341.2:p.His922Asp
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