Canonical Allele Identifier: CA2360861645
Gene: E2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675479G= , CM000682.2:g.33675479G= GRCh38
NC_000020.10:g.32263285G= , CM000682.1:g.32263285G= GRCh37
NC_000020.9:g.31726946G= NCBI36
NG_046988.1:g.15926C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1253C= MANE Select ENSP00000345571.5:n.*1253C=
NM_005225.3:c.*1253C= MANE Select NP_005216.1:n.*1253C=