Canonical Allele Identifier: CA2082579334

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872776T= , CM000675.2:g.31872776T= GRCh38
NC_000013.10:g.32446913T= , CM000675.1:g.32446913T= GRCh37
NC_000013.9:g.31344913T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645780.1:c.-254+25837T= (FRY) ENSP00000494080.1:n.-254+25837T=
ENST00000428783.1:n.99+25837T= (EEF1DP3)
NR_027062.1:n.157+25837T= (EEF1DP3)