Canonical Allele Identifier: CA26837884
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs115801024
gnomAD v4: 1-94010641-G-C
MyVariant Identifiers: chr1:g.94476197G>C (hg19) chr1:g.94010641G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94010641G>C , CM000663.2:g.94010641G>C GRCh38
NC_000001.10:g.94476197G>C , CM000663.1:g.94476197G>C GRCh37
NC_000001.9:g.94248785G>C NCBI36
NG_009073.1:g.115509C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5714+159C>G MANE Select ENSP00000359245.3:n.5714+159C>G
ENST00000370225.3:c.5714+159C>G ENSP00000359245.3:n.5714+159C>G
ENST00000465352.1:n.130+159C>G
ENST00000536513.5:c.2090+159C>G ENSP00000439707.2:n.2090+159C>G
NM_000350.2:c.5714+159C>G NP_000341.2:n.5714+159C>G
NM_000350.3:c.5714+159C>G MANE Select NP_000341.2:n.5714+159C>G
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