Canonical Allele Identifier: CA418812398
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94512633A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047077A>C , CM000663.2:g.94047077A>C GRCh38
NC_000001.10:g.94512633A>C , CM000663.1:g.94512633A>C GRCh37
NC_000001.9:g.94285221A>C NCBI36
NG_009073.1:g.79073T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2760T>G MANE Select ENSP00000359245.3:p.Arg920=
ENST00000649773.1:c.2538T>G ENSP00000496882.1:p.Arg846=
ENST00000370225.3:c.2760T>G ENSP00000359245.3:p.Arg920=
ENST00000536513.5:c.-64-6988T>G ENSP00000439707.2:n.-64-6988T>G
NM_000350.2:c.2760T>G NP_000341.2:p.Arg920=
NM_000350.3:c.2760T>G MANE Select NP_000341.2:p.Arg920=
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Search 100 bp 3'