Canonical Allele Identifier: CA418821722
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94486891G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021335G>T , CM000663.2:g.94021335G>T GRCh38
NC_000001.10:g.94486891G>T , CM000663.1:g.94486891G>T GRCh37
NC_000001.9:g.94259479G>T NCBI36
NG_009073.1:g.104815C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4923C>A MANE Select ENSP00000359245.3:p.Ala1641=
ENST00000370225.3:c.4923C>A ENSP00000359245.3:p.Ala1641=
ENST00000460514.1:n.417C>A
ENST00000470771.1:n.33C>A
ENST00000536513.5:c.1299C>A ENSP00000439707.2:p.Ala433=
NM_000350.2:c.4923C>A NP_000341.2:p.Ala1641=
NM_000350.3:c.4923C>A MANE Select NP_000341.2:p.Ala1641=
Search 100 bp 5'
Search 100 bp 3'