Canonical Allele Identifier: CA1004558916
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1660208264
gnomAD v3: 1-94031718-G-A
gnomAD v4: 1-94031718-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94031718G>A , CM000663.2:g.94031718G>A GRCh38
NC_000001.10:g.94497274G>A , CM000663.1:g.94497274G>A GRCh37
NC_000001.9:g.94269862G>A NCBI36
NG_009073.1:g.94432C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4128+60C>T MANE Select ENSP00000359245.3:n.4128+60C>T
ENST00000370225.3:c.4128+60C>T ENSP00000359245.3:n.4128+60C>T
ENST00000536513.5:c.504+60C>T ENSP00000439707.2:n.504+60C>T
NM_000350.2:c.4128+60C>T NP_000341.2:n.4128+60C>T
NM_000350.3:c.4128+60C>T MANE Select NP_000341.2:n.4128+60C>T
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