Canonical Allele Identifier: CA60446138
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs955118195
MyVariant Identifiers: chr2:g.168811404A>G (hg19) chr2:g.167954894A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954894A>G , CM000664.2:g.167954894A>G GRCh38
NC_000002.11:g.168811404A>G , CM000664.1:g.168811404A>G GRCh37
NC_000002.10:g.168519650A>G NCBI36
NG_052783.1:g.297702T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2177T>C ENSP00000513185.1:n.2177T>C
ENST00000355999.5:c.*602T>C MANE Select ENSP00000348278.4:n.*602T>C
ENST00000355999.4:c.*602T>C ENSP00000348278.4:n.*602T>C
ENST00000487143.5:n.1340T>C
NM_013233.2:c.*602T>C NP_037365.2:n.*602T>C
XM_005246465.2:c.*602T>C XP_005246522.1:n.*602T>C
XM_011510966.1:c.*602T>C XP_011509268.1:n.*602T>C
XM_011510967.1:c.*602T>C XP_011509269.1:n.*602T>C
NM_013233.3:c.*602T>C MANE Select NP_037365.2:n.*602T>C
Search 100 bp 5'
Search 100 bp 3'