Canonical Allele Identifier: CA516683725
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487646T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744550T>A , CM000685.2:g.51744550T>A GRCh38
NC_000023.10:g.51487646T>A , CM000685.1:g.51487646T>A GRCh37
NC_000023.9:g.51504386T>A NCBI36
NG_016857.1:g.6166T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.924T>A MANE Select ENSP00000341247.4:p.Ala308=
ENST00000340438.5:c.924T>A ENSP00000341247.4:p.Ala308=
NM_018094.4:c.924T>A NP_060564.2:p.Ala308=
NM_018094.5:c.924T>A MANE Select NP_060564.2:p.Ala308=
Search 100 bp 5'
Search 100 bp 3'