Canonical Allele Identifier: CA524697506
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1451099631
gnomAD v2: 1-94512354-G-T
gnomAD v3: 1-94046798-G-T
gnomAD v4: 1-94046798-G-T
MyVariant Identifiers: chr1:g.94512354G>T (hg19) chr1:g.94046798G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046798G>T , CM000663.2:g.94046798G>T GRCh38
NC_000001.10:g.94512354G>T , CM000663.1:g.94512354G>T GRCh37
NC_000001.9:g.94284942G>T NCBI36
NG_009073.1:g.79352C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.2918+121C>A MANE Select ENSP00000359245.3:n.2918+121C>A
ENST00000649773.1:c.2696+121C>A ENSP00000496882.1:n.2696+121C>A
ENST00000370225.3:c.2918+121C>A ENSP00000359245.3:n.2918+121C>A
ENST00000536513.5:c.-64-6709C>A ENSP00000439707.2:n.-64-6709C>A
NM_000350.2:c.2918+121C>A NP_000341.2:n.2918+121C>A
NM_000350.3:c.2918+121C>A MANE Select NP_000341.2:n.2918+121C>A
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