Canonical Allele Identifier: CA760392608
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs1328688058
MyVariant Identifiers: chr2:g.168811409A>G (hg19) chr2:g.167954899A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954899A>G , CM000664.2:g.167954899A>G GRCh38
NC_000002.11:g.168811409A>G , CM000664.1:g.168811409A>G GRCh37
NC_000002.10:g.168519655A>G NCBI36
NG_052783.1:g.297697T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2172T>C ENSP00000513185.1:n.2172T>C
ENST00000355999.5:c.*597T>C MANE Select ENSP00000348278.4:n.*597T>C
ENST00000355999.4:c.*597T>C ENSP00000348278.4:n.*597T>C
ENST00000487143.5:n.1335T>C
NM_013233.2:c.*597T>C NP_037365.2:n.*597T>C
XM_005246465.2:c.*597T>C XP_005246522.1:n.*597T>C
XM_011510966.1:c.*597T>C XP_011509268.1:n.*597T>C
XM_011510967.1:c.*597T>C XP_011509269.1:n.*597T>C
NM_013233.3:c.*597T>C MANE Select NP_037365.2:n.*597T>C
Search 100 bp 5'
Search 100 bp 3'