Canonical Allele Identifier: CA341286032
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94030999-A-G
MyVariant Identifiers: chr1:g.94496555A>G (hg19) chr1:g.94030999A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030999A>G , CM000663.2:g.94030999A>G GRCh38
NC_000001.10:g.94496555A>G , CM000663.1:g.94496555A>G GRCh37
NC_000001.9:g.94269143A>G NCBI36
NG_009073.1:g.95151T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4250T>C MANE Select ENSP00000359245.3:p.Phe1417Ser
ENST00000370225.3:c.4250T>C ENSP00000359245.3:p.Phe1417Ser
ENST00000536513.5:c.626T>C ENSP00000439707.2:p.Phe209Ser
NM_000350.2:c.4250T>C NP_000341.2:p.Phe1417Ser
NM_000350.3:c.4250T>C MANE Select NP_000341.2:p.Phe1417Ser
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