Canonical Allele Identifier: CA247943088
Gene: FRY HGNC NCBI
EEF1DP3 HGNC NCBI

Linked Data

dbSNP Id: rs190904692
gnomAD v3: 13-31872584-T-A
gnomAD v4: 13-31872584-T-A
MyVariant Identifiers: chr13:g.32446721T>A (hg19) chr13:g.31872584T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872584T>A , CM000675.2:g.31872584T>A GRCh38
NC_000013.10:g.32446721T>A , CM000675.1:g.32446721T>A GRCh37
NC_000013.9:g.31344721T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25645T>A (FRY) ENSP00000494080.1:n.-254+25645T>A
ENST00000428783.1:n.99+25645T>A (EEF1DP3)
NR_027062.1:n.157+25645T>A (EEF1DP3)
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