Canonical Allele Identifier: CA413207711
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487749C>G (hg19) chrX:g.51744653C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744653C>G , CM000685.2:g.51744653C>G GRCh38
NC_000023.10:g.51487749C>G , CM000685.1:g.51487749C>G GRCh37
NC_000023.9:g.51504489C>G NCBI36
NG_016857.1:g.6269C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.1027C>G MANE Select ENSP00000341247.4:p.His343Asp
ENST00000340438.5:c.1027C>G ENSP00000341247.4:p.His343Asp
NM_018094.4:c.1027C>G NP_060564.2:p.His343Asp
NM_018094.5:c.1027C>G MANE Select NP_060564.2:p.His343Asp
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Search 100 bp 3'