Canonical Allele Identifier: CA341283160
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94021371-G-T
MyVariant Identifiers: chr1:g.94486927G>T (hg19) chr1:g.94021371G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021371G>T , CM000663.2:g.94021371G>T GRCh38
NC_000001.10:g.94486927G>T , CM000663.1:g.94486927G>T GRCh37
NC_000001.9:g.94259515G>T NCBI36
NG_009073.1:g.104779C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4887C>A MANE Select ENSP00000359245.3:p.Ser1629Arg
ENST00000370225.3:c.4887C>A ENSP00000359245.3:p.Ser1629Arg
ENST00000460514.1:n.381C>A
ENST00000536513.5:c.1263C>A ENSP00000439707.2:p.Ser421Arg
NM_000350.2:c.4887C>A NP_000341.2:p.Ser1629Arg
NM_000350.3:c.4887C>A MANE Select NP_000341.2:p.Ser1629Arg
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Search 100 bp 3'