Canonical Allele Identifier: CA2646650037
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94043499-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043499A>C , CM000663.2:g.94043499A>C GRCh38
NC_000001.10:g.94509055A>C , CM000663.1:g.94509055A>C GRCh37
NC_000001.9:g.94281643A>C NCBI36
NG_009073.1:g.82651T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3051-24T>G MANE Select ENSP00000359245.3:n.3051-24T>G
ENST00000370225.3:c.3051-24T>G ENSP00000359245.3:n.3051-24T>G
ENST00000536513.5:c.-64-3410T>G ENSP00000439707.2:n.-64-3410T>G
NM_000350.2:c.3051-24T>G NP_000341.2:n.3051-24T>G
NM_000350.3:c.3051-24T>G MANE Select NP_000341.2:n.3051-24T>G