Canonical Allele Identifier: CA12250047
Gene: SGK1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11755699

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134278109T>C , CM000668.2:g.134278109T>C GRCh38
NC_000006.11:g.134599247T>C , CM000668.1:g.134599247T>C GRCh37
NC_000006.10:g.134640940T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001143676.1:c.70-15961A>G VV NP_001137148.1:p.=
XM_011536071.1:c.70-15961A>G XP_011534373.1:p.=
ENST00000367858.9:c.70-15961A>G ENSP00000356832.5:p.=
ENST00000461976.2:c.-24-15961A>G ENSP00000435577.1:p.=
ENST00000524929.1:c.70-15961A>G ENSP00000435724.1:p.=
ENST00000533224.1:c.70-15961A>G ENSP00000436470.1:p.=