Canonical Allele Identifier: CA2082579362

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872803T= , CM000675.2:g.31872803T= GRCh38
NC_000013.10:g.32446940T= , CM000675.1:g.32446940T= GRCh37
NC_000013.9:g.31344940T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25864T= (FRY) ENSP00000494080.1:n.-254+25864T=
ENST00000428783.1:n.99+25864T= (EEF1DP3)
NR_027062.1:n.157+25864T= (EEF1DP3)