Canonical Allele Identifier: CA341278313
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94467507G>C (hg19) chr1:g.94001951G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001951G>C , CM000663.2:g.94001951G>C GRCh38
NC_000001.10:g.94467507G>C , CM000663.1:g.94467507G>C GRCh37
NC_000001.9:g.94240095G>C NCBI36
NG_009073.1:g.124199C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6189C>G MANE Select ENSP00000359245.3:p.Tyr2063Ter
ENST00000370225.3:c.6189C>G ENSP00000359245.3:p.Tyr2063Ter
ENST00000465352.1:n.605C>G
ENST00000536513.5:c.2565C>G ENSP00000439707.2:p.Tyr855Ter
NM_000350.2:c.6189C>G NP_000341.2:p.Tyr2063Ter
NM_000350.3:c.6189C>G MANE Select NP_000341.2:p.Tyr2063Ter
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