Canonical Allele Identifier: CA2646650011
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94031710-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94031710T>C , CM000663.2:g.94031710T>C GRCh38
NC_000001.10:g.94497266T>C , CM000663.1:g.94497266T>C GRCh37
NC_000001.9:g.94269854T>C NCBI36
NG_009073.1:g.94440A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4128+68A>G MANE Select ENSP00000359245.3:n.4128+68A>G
ENST00000370225.3:c.4128+68A>G ENSP00000359245.3:n.4128+68A>G
ENST00000536513.5:c.504+68A>G ENSP00000439707.2:n.504+68A>G
NM_000350.2:c.4128+68A>G NP_000341.2:n.4128+68A>G
NM_000350.3:c.4128+68A>G MANE Select NP_000341.2:n.4128+68A>G