Canonical Allele Identifier: CA467493766
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576401C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814122C>G , CM000671.2:g.129814122C>G GRCh38
NC_000009.11:g.132576401C>G , CM000671.1:g.132576401C>G GRCh37
NC_000009.10:g.131616222C>G NCBI36
NG_008049.1:g.15041G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.849G>C MANE Select ENSP00000345719.4:p.Val283=
ENST00000651202.1:c.*117G>C ENSP00000498222.1:n.*117G>C
ENST00000351698.4:c.849G>C ENSP00000345719.4:p.Val283=
ENST00000474192.1:n.433G>C
NM_000113.2:c.849G>C NP_000104.1:p.Val283=
XR_929731.1:n.1176G>C
XR_929731.3:n.1044G>C
NM_000113.3:c.849G>C MANE Select NP_000104.1:p.Val283=
Search 100 bp 5'
Search 100 bp 3'