Canonical Allele Identifier: CA2360861684
Gene: E2F1 HGNC NCBI

Linked Data

dbSNP Id: rs2017939449
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675597A>C , CM000682.2:g.33675597A>C GRCh38
NC_000020.10:g.32263403A>C , CM000682.1:g.32263403A>C GRCh37
NC_000020.9:g.31727064A>C NCBI36
NG_046988.1:g.15808T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1135T>G MANE Select ENSP00000345571.5:n.*1135T>G
NM_005225.2:c.*1135T>G NP_005216.1:n.*1135T>G
NM_005225.3:c.*1135T>G MANE Select NP_005216.1:n.*1135T>G
Search 100 bp 5'
Search 100 bp 3'