Canonical Allele Identifier: CA2082579158

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872625C= , CM000675.2:g.31872625C= GRCh38
NC_000013.10:g.32446762C= , CM000675.1:g.32446762C= GRCh37
NC_000013.9:g.31344762C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25686C= (FRY) ENSP00000494080.1:n.-254+25686C=
ENST00000428783.1:n.99+25686C= (EEF1DP3)
NR_027062.1:n.157+25686C= (EEF1DP3)