Canonical Allele Identifier: CA200533482
Gene: TOR1A HGNC NCBI

Linked Data

dbSNP Id: rs569910379
gnomAD v3: 9-129813529-T-C
gnomAD v4: 9-129813529-T-C
MyVariant Identifiers: chr9:g.132575808T>C (hg19) chr9:g.129813529T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129813529T>C , CM000671.2:g.129813529T>C GRCh38
NC_000009.11:g.132575808T>C , CM000671.1:g.132575808T>C GRCh37
NC_000009.10:g.131615629T>C NCBI36
NG_008049.1:g.15634A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.*443A>G MANE Select ENSP00000345719.4:n.*443A>G
ENST00000651202.1:c.*710A>G ENSP00000498222.1:n.*710A>G
ENST00000351698.4:c.*443A>G ENSP00000345719.4:n.*443A>G
NM_000113.2:c.*443A>G NP_000104.1:n.*443A>G
XR_929731.3:n.1637A>G
NM_000113.3:c.*443A>G MANE Select NP_000104.1:n.*443A>G
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