Canonical Allele Identifier: CA375199342
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132581166T>C (hg19) chr9:g.129818887T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129818887T>C , CM000671.2:g.129818887T>C GRCh38
NC_000009.11:g.132581166T>C , CM000671.1:g.132581166T>C GRCh37
NC_000009.10:g.131620987T>C NCBI36
NG_008049.1:g.10276A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.478A>G MANE Select ENSP00000345719.4:p.Ser160Gly
ENST00000651202.1:c.574A>G ENSP00000498222.1:p.Ser192Gly
ENST00000351698.4:c.478A>G ENSP00000345719.4:p.Ser160Gly
ENST00000473604.2:n.588A>G
NM_000113.2:c.478A>G NP_000104.1:p.Ser160Gly
XR_929731.1:n.638A>G
XR_929731.3:n.506A>G
NM_000113.3:c.478A>G MANE Select NP_000104.1:p.Ser160Gly
Search 100 bp 5'
Search 100 bp 3'