Canonical Allele Identifier: CA341284776
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2697215
ClinVar RCV Id: RCV003549166
dbSNP Id: rs1316934987
gnomAD v4: 1-94029453-G-T
MyVariant Identifiers: chr1:g.94495009G>T (hg19) chr1:g.94029453G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029453G>T , CM000663.2:g.94029453G>T GRCh38
NC_000001.10:g.94495009G>T , CM000663.1:g.94495009G>T GRCh37
NC_000001.9:g.94267597G>T NCBI36
NG_009073.1:g.96697C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4531C>A MANE Select ENSP00000359245.3:p.Pro1511Thr
ENST00000370225.3:c.4531C>A ENSP00000359245.3:p.Pro1511Thr
ENST00000536513.5:c.907C>A ENSP00000439707.2:p.Pro303Thr
NM_000350.2:c.4531C>A NP_000341.2:p.Pro1511Thr
NM_000350.3:c.4531C>A MANE Select NP_000341.2:p.Pro1511Thr
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