Canonical Allele Identifier: CA467493867
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576452A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814173A>G , CM000671.2:g.129814173A>G GRCh38
NC_000009.11:g.132576452A>G , CM000671.1:g.132576452A>G GRCh37
NC_000009.10:g.131616273A>G NCBI36
NG_008049.1:g.14990T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.798T>C MANE Select ENSP00000345719.4:p.Phe266=
ENST00000651202.1:c.*66T>C ENSP00000498222.1:n.*66T>C
ENST00000351698.4:c.798T>C ENSP00000345719.4:p.Phe266=
ENST00000474192.1:n.382T>C
NM_000113.2:c.798T>C NP_000104.1:p.Phe266=
XR_929731.1:n.1125T>C
XR_929731.3:n.993T>C
NM_000113.3:c.798T>C MANE Select NP_000104.1:p.Phe266=
Search 100 bp 5'
Search 100 bp 3'