Canonical Allele Identifier: CA516683889
Gene: GSPT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.51487745A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51744649A>C , CM000685.2:g.51744649A>C GRCh38
NC_000023.10:g.51487745A>C , CM000685.1:g.51487745A>C GRCh37
NC_000023.9:g.51504485A>C NCBI36
NG_016857.1:g.6265A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340438.6:c.1023A>C MANE Select ENSP00000341247.4:p.Val341=
ENST00000340438.5:c.1023A>C ENSP00000341247.4:p.Val341=
NM_018094.4:c.1023A>C NP_060564.2:p.Val341=
NM_018094.5:c.1023A>C MANE Select NP_060564.2:p.Val341=
Search 100 bp 5'
Search 100 bp 3'