Canonical Allele Identifier: CA341285392
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94577017A>C (hg19) chr1:g.94111461A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111461A>C , CM000663.2:g.94111461A>C GRCh38
NC_000001.10:g.94577017A>C , CM000663.1:g.94577017A>C GRCh37
NC_000001.9:g.94349605A>C NCBI36
NG_009073.1:g.14689T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.279T>G MANE Select ENSP00000359245.3:p.Ile93Met
ENST00000649773.1:c.279T>G ENSP00000496882.1:p.Ile93Met
ENST00000370225.3:c.279T>G ENSP00000359245.3:p.Ile93Met
NM_000350.2:c.279T>G NP_000341.2:p.Ile93Met
NM_000350.3:c.279T>G MANE Select NP_000341.2:p.Ile93Met
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