Canonical Allele Identifier: CA467494109
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132581194C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129818915C>T , CM000671.2:g.129818915C>T GRCh38
NC_000009.11:g.132581194C>T , CM000671.1:g.132581194C>T GRCh37
NC_000009.10:g.131621015C>T NCBI36
NG_008049.1:g.10248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.450G>A MANE Select ENSP00000345719.4:p.Gln150=
ENST00000651202.1:c.546G>A ENSP00000498222.1:p.Gln182=
ENST00000351698.4:c.450G>A ENSP00000345719.4:p.Gln150=
ENST00000473604.2:n.560G>A
NM_000113.2:c.450G>A NP_000104.1:p.Gln150=
XR_929731.1:n.610G>A
XR_929731.3:n.478G>A
NM_000113.3:c.450G>A MANE Select NP_000104.1:p.Gln150=
Search 100 bp 5'
Search 100 bp 3'