Canonical Allele Identifier: CA1004563091
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1660470452
gnomAD v3: 1-94040999-T-G
gnomAD v4: 1-94040999-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94040999T>G , CM000663.2:g.94040999T>G GRCh38
NC_000001.10:g.94506555T>G , CM000663.1:g.94506555T>G GRCh37
NC_000001.9:g.94279143T>G NCBI36
NG_009073.1:g.85151A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3522+210A>C MANE Select ENSP00000359245.3:n.3522+210A>C
ENST00000370225.3:c.3522+210A>C ENSP00000359245.3:n.3522+210A>C
ENST00000536513.5:c.-64-910A>C ENSP00000439707.2:n.-64-910A>C
NM_000350.2:c.3522+210A>C NP_000341.2:n.3522+210A>C
NM_000350.3:c.3522+210A>C MANE Select NP_000341.2:n.3522+210A>C
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