Canonical Allele Identifier: CA2360861655
Gene: E2F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675510T= , CM000682.2:g.33675510T= GRCh38
NC_000020.10:g.32263316T= , CM000682.1:g.32263316T= GRCh37
NC_000020.9:g.31726977T= NCBI36
NG_046988.1:g.15895A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1222A= MANE Select ENSP00000345571.5:n.*1222A=
NM_005225.2:c.*1222A= NP_005216.1:n.*1222A=
NM_005225.3:c.*1222A= MANE Select NP_005216.1:n.*1222A=
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