Canonical Allele Identifier: CA2360861646
Gene: E2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675484T= , CM000682.2:g.33675484T= GRCh38
NC_000020.10:g.32263290T= , CM000682.1:g.32263290T= GRCh37
NC_000020.9:g.31726951T= NCBI36
NG_046988.1:g.15921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1248A= MANE Select ENSP00000345571.5:n.*1248A=
NM_005225.3:c.*1248A= MANE Select NP_005216.1:n.*1248A=