Canonical Allele Identifier: CA313282758
Gene: E2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1007241903
MyVariant Identifiers: chr20:g.32263377A>G (hg19) chr20:g.33675571A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675571A>G , CM000682.2:g.33675571A>G GRCh38
NC_000020.10:g.32263377A>G , CM000682.1:g.32263377A>G GRCh37
NC_000020.9:g.31727038A>G NCBI36
NG_046988.1:g.15834T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1161T>C MANE Select ENSP00000345571.5:n.*1161T>C
NM_005225.2:c.*1161T>C NP_005216.1:n.*1161T>C
NM_005225.3:c.*1161T>C MANE Select NP_005216.1:n.*1161T>C
Search 100 bp 5'
Search 100 bp 3'