Canonical Allele Identifier: CA2646650036
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94043497-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043497A>G , CM000663.2:g.94043497A>G GRCh38
NC_000001.10:g.94509053A>G , CM000663.1:g.94509053A>G GRCh37
NC_000001.9:g.94281641A>G NCBI36
NG_009073.1:g.82653T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3051-22T>C MANE Select ENSP00000359245.3:n.3051-22T>C
ENST00000370225.3:c.3051-22T>C ENSP00000359245.3:n.3051-22T>C
ENST00000536513.5:c.-64-3408T>C ENSP00000439707.2:n.-64-3408T>C
NM_000350.2:c.3051-22T>C NP_000341.2:n.3051-22T>C
NM_000350.3:c.3051-22T>C MANE Select NP_000341.2:n.3051-22T>C