Canonical Allele Identifier: CA819293521
Gene: SGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1008697356
gnomAD v3: 6-134278029-G-T
gnomAD v4: 6-134278029-G-T
MyVariant Identifiers: chr6:g.134599167G>T (hg19) chr6:g.134278029G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134278029G>T , CM000668.2:g.134278029G>T GRCh38
NC_000006.11:g.134599167G>T , CM000668.1:g.134599167G>T GRCh37
NC_000006.10:g.134640860G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367858.10:c.70-15881C>A MANE Select ENSP00000356832.5:n.70-15881C>A
ENST00000367858.9:c.70-15881C>A ENSP00000356832.5:n.70-15881C>A
ENST00000461976.2:c.-24-15881C>A ENSP00000435577.1:n.-24-15881C>A
ENST00000524929.1:c.70-15881C>A ENSP00000435724.1:n.70-15881C>A
ENST00000533224.1:c.70-15881C>A ENSP00000436470.1:n.70-15881C>A
NM_001143676.1:c.70-15881C>A NP_001137148.1:n.70-15881C>A
XM_011536071.1:c.70-15881C>A XP_011534373.1:n.70-15881C>A
NM_001143676.3:c.70-15881C>A MANE Select NP_001137148.1:n.70-15881C>A
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