Canonical Allele Identifier: CA2360861658
Gene: E2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675529A= , CM000682.2:g.33675529A= GRCh38
NC_000020.10:g.32263335A= , CM000682.1:g.32263335A= GRCh37
NC_000020.9:g.31726996A= NCBI36
NG_046988.1:g.15876T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1203T= MANE Select ENSP00000345571.5:n.*1203T=
NM_005225.2:c.*1203T= NP_005216.1:n.*1203T=
NM_005225.3:c.*1203T= MANE Select NP_005216.1:n.*1203T=