Canonical Allele Identifier: CA15982001
Gene: ETS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1051476

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.38823912C>G , CM000683.2:g.38823912C>G GRCh38
NC_000021.8:g.40195836C>G , CM000683.1:g.40195836C>G GRCh37
NC_000021.7:g.39117706C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001256295.1:c.*1023C>G VV NP_001243224.1:p.=
NM_005239.5:c.*1023C>G VV NP_005230.1:p.=
XM_005260935.1:c.*1023C>G XP_005260992.1:p.=
XM_017028290.1:c.*1023C>G XP_016883779.1:p.=
NM_005239.6:c.*1023C>G VV MANE Preferred
ENST00000360214.7:c.*1023C>G ENSP00000353344.3:p.=
ENST00000360938.7:c.*1023C>G ENSP00000354194.3:p.=