Canonical Allele Identifier: CA375197951
Gene: TOR1A HGNC NCBI

Linked Data

dbSNP Id: rs1463399739
MyVariant Identifiers: chr9:g.132576459T>A (hg19) chr9:g.129814180T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814180T>A , CM000671.2:g.129814180T>A GRCh38
NC_000009.11:g.132576459T>A , CM000671.1:g.132576459T>A GRCh37
NC_000009.10:g.131616280T>A NCBI36
NG_008049.1:g.14983A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.791A>T MANE Select ENSP00000345719.4:p.Asp264Val
ENST00000651202.1:c.*59A>T ENSP00000498222.1:n.*59A>T
ENST00000351698.4:c.791A>T ENSP00000345719.4:p.Asp264Val
ENST00000474192.1:n.375A>T
NM_000113.2:c.791A>T NP_000104.1:p.Asp264Val
XR_929731.1:n.1118A>T
XR_929731.3:n.986A>T
NM_000113.3:c.791A>T MANE Select NP_000104.1:p.Asp264Val
Search 100 bp 5'
Search 100 bp 3'