Canonical Allele Identifier: CA413207491
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487654T>G (hg19) chrX:g.51744558T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744558T>G , CM000685.2:g.51744558T>G GRCh38
NC_000023.10:g.51487654T>G , CM000685.1:g.51487654T>G GRCh37
NC_000023.9:g.51504394T>G NCBI36
NG_016857.1:g.6174T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.932T>G MANE Select ENSP00000341247.4:p.Val311Gly
ENST00000340438.5:c.932T>G ENSP00000341247.4:p.Val311Gly
NM_018094.4:c.932T>G NP_060564.2:p.Val311Gly
NM_018094.5:c.932T>G MANE Select NP_060564.2:p.Val311Gly
Search 100 bp 5'
Search 100 bp 3'