Canonical Allele Identifier: CA26836714
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1047039873
MyVariant Identifiers: chr1:g.94007599G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94007599G>C , CM000663.2:g.94007599G>C GRCh38
NC_000001.10:g.94473155G>C , CM000663.1:g.94473155G>C GRCh37
NC_000001.9:g.94245743G>C NCBI36
NG_009073.1:g.118551C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6005+35C>G MANE Select ENSP00000359245.3:n.6005+35C>G
ENST00000370225.3:c.6005+35C>G ENSP00000359245.3:n.6005+35C>G
ENST00000465352.1:n.421+35C>G
ENST00000484388.1:n.119+35C>G
ENST00000536513.5:c.2381+35C>G ENSP00000439707.2:n.2381+35C>G
NM_000350.2:c.6005+35C>G NP_000341.2:n.6005+35C>G
NM_000350.3:c.6005+35C>G MANE Select NP_000341.2:n.6005+35C>G
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