Canonical Allele Identifier: CA341291159
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038984
ClinVar RCV Id: RCV001342373
dbSNP Id: rs1660481292
gnomAD v4: 1-94041355-G-C
MyVariant Identifiers: chr1:g.94506911G>C (hg19) chr1:g.94041355G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041355G>C , CM000663.2:g.94041355G>C GRCh38
NC_000001.10:g.94506911G>C , CM000663.1:g.94506911G>C GRCh37
NC_000001.9:g.94279499G>C NCBI36
NG_009073.1:g.84795C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3376C>G MANE Select ENSP00000359245.3:p.Leu1126Val
ENST00000370225.3:c.3376C>G ENSP00000359245.3:p.Leu1126Val
ENST00000536513.5:c.-64-1266C>G ENSP00000439707.2:n.-64-1266C>G
NM_000350.2:c.3376C>G NP_000341.2:p.Leu1126Val
NM_000350.3:c.3376C>G MANE Select NP_000341.2:p.Leu1126Val
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