Canonical Allele Identifier: CA413207489
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487653G>T (hg19) chrX:g.51744557G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744557G>T , CM000685.2:g.51744557G>T GRCh38
NC_000023.10:g.51487653G>T , CM000685.1:g.51487653G>T GRCh37
NC_000023.9:g.51504393G>T NCBI36
NG_016857.1:g.6173G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.931G>T MANE Select ENSP00000341247.4:p.Val311Phe
ENST00000340438.5:c.931G>T ENSP00000341247.4:p.Val311Phe
NM_018094.4:c.931G>T NP_060564.2:p.Val311Phe
NM_018094.5:c.931G>T MANE Select NP_060564.2:p.Val311Phe
Search 100 bp 5'
Search 100 bp 3'