Canonical Allele Identifier: CA2646646371
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94008218-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94008218G>T , CM000663.2:g.94008218G>T GRCh38
NC_000001.10:g.94473774G>T , CM000663.1:g.94473774G>T GRCh37
NC_000001.9:g.94246362G>T NCBI36
NG_009073.1:g.117932C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5898+17C>A MANE Select ENSP00000359245.3:n.5898+17C>A
ENST00000370225.3:c.5898+17C>A ENSP00000359245.3:n.5898+17C>A
ENST00000465352.1:n.314+17C>A
ENST00000536513.5:c.2274+17C>A ENSP00000439707.2:n.2274+17C>A
NM_000350.2:c.5898+17C>A NP_000341.2:n.5898+17C>A
NM_000350.3:c.5898+17C>A MANE Select NP_000341.2:n.5898+17C>A
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