Canonical Allele Identifier: CA1181408489
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1659899739
gnomAD v4: 1-94021626-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021626C>T , CM000663.2:g.94021626C>T GRCh38
NC_000001.10:g.94487182C>T , CM000663.1:g.94487182C>T GRCh37
NC_000001.9:g.94259770C>T NCBI36
NG_009073.1:g.104524G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4848+14G>A MANE Select ENSP00000359245.3:n.4848+14G>A
ENST00000370225.3:c.4848+14G>A ENSP00000359245.3:n.4848+14G>A
ENST00000460514.1:n.342+14G>A
ENST00000536513.5:c.1224+14G>A ENSP00000439707.2:n.1224+14G>A
NM_000350.2:c.4848+14G>A NP_000341.2:n.4848+14G>A
NM_000350.3:c.4848+14G>A MANE Select NP_000341.2:n.4848+14G>A
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