Canonical Allele Identifier: CA26853268
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1015495836
gnomAD v2: 1-94494862-T-C
gnomAD v3: 1-94029306-T-C
gnomAD v4: 1-94029306-T-C
MyVariant Identifiers: chr1:g.94494862T>C (hg19) chr1:g.94029306T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029306T>C , CM000663.2:g.94029306T>C GRCh38
NC_000001.10:g.94494862T>C , CM000663.1:g.94494862T>C GRCh37
NC_000001.9:g.94267450T>C NCBI36
NG_009073.1:g.96844A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4539+139A>G MANE Select ENSP00000359245.3:n.4539+139A>G
ENST00000370225.3:c.4539+139A>G ENSP00000359245.3:n.4539+139A>G
ENST00000536513.5:c.915+139A>G ENSP00000439707.2:n.915+139A>G
NM_000350.2:c.4539+139A>G NP_000341.2:n.4539+139A>G
NM_000350.3:c.4539+139A>G MANE Select NP_000341.2:n.4539+139A>G
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