Canonical Allele Identifier: CA2580063570
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2429001
ClinVar RCV Id: RCV003123242

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011395A>C , CM000663.2:g.94011395A>C GRCh38
NC_000001.10:g.94476951A>C , CM000663.1:g.94476951A>C GRCh37
NC_000001.9:g.94249539A>C NCBI36
NG_009073.1:g.114755T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5461-10T>G MANE Select ENSP00000359245.3:n.5461-10T>G
ENST00000370225.3:c.5461-10T>G ENSP00000359245.3:n.5461-10T>G
ENST00000536513.5:c.1837-10T>G ENSP00000439707.2:n.1837-10T>G
NM_000350.2:c.5461-10T>G NP_000341.2:n.5461-10T>G
NM_000350.3:c.5461-10T>G MANE Select NP_000341.2:n.5461-10T>G