Canonical Allele Identifier: CA26836702
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs934019986
gnomAD v3: 1-94007575-C-T
gnomAD v4: 1-94007575-C-T
MyVariant Identifiers: chr1:g.94473131C>T (hg19) chr1:g.94007575C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94007575C>T , CM000663.2:g.94007575C>T GRCh38
NC_000001.10:g.94473131C>T , CM000663.1:g.94473131C>T GRCh37
NC_000001.9:g.94245719C>T NCBI36
NG_009073.1:g.118575G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6005+59G>A MANE Select ENSP00000359245.3:n.6005+59G>A
ENST00000370225.3:c.6005+59G>A ENSP00000359245.3:n.6005+59G>A
ENST00000465352.1:n.421+59G>A
ENST00000484388.1:n.119+59G>A
ENST00000536513.5:c.2381+59G>A ENSP00000439707.2:n.2381+59G>A
NM_000350.2:c.6005+59G>A NP_000341.2:n.6005+59G>A
NM_000350.3:c.6005+59G>A MANE Select NP_000341.2:n.6005+59G>A
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