Canonical Allele Identifier: CA26836692
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs996641380
MyVariant Identifiers: chr1:g.94473111G>A (hg19) chr1:g.94007555G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94007555G>A , CM000663.2:g.94007555G>A GRCh38
NC_000001.10:g.94473111G>A , CM000663.1:g.94473111G>A GRCh37
NC_000001.9:g.94245699G>A NCBI36
NG_009073.1:g.118595C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6005+79C>T MANE Select ENSP00000359245.3:n.6005+79C>T
ENST00000370225.3:c.6005+79C>T ENSP00000359245.3:n.6005+79C>T
ENST00000465352.1:n.421+79C>T
ENST00000484388.1:n.119+79C>T
ENST00000536513.5:c.2381+79C>T ENSP00000439707.2:n.2381+79C>T
NM_000350.2:c.6005+79C>T NP_000341.2:n.6005+79C>T
NM_000350.3:c.6005+79C>T MANE Select NP_000341.2:n.6005+79C>T
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