Canonical Allele Identifier: CA590944207
Gene: TOR1A HGNC NCBI

Linked Data

dbSNP Id: rs1466136128
gnomAD v2: 9-132581364-G-C
gnomAD v3: 9-129819085-G-C
gnomAD v4: 9-129819085-G-C
MyVariant Identifiers: chr9:g.132581364G>C (hg19) chr9:g.129819085G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129819085G>C , CM000671.2:g.129819085G>C GRCh38
NC_000009.11:g.132581364G>C , CM000671.1:g.132581364G>C GRCh37
NC_000009.10:g.131621185G>C NCBI36
NG_008049.1:g.10078C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.445-165C>G MANE Select ENSP00000345719.4:n.445-165C>G
ENST00000651202.1:c.541-165C>G ENSP00000498222.1:n.541-165C>G
ENST00000351698.4:c.445-165C>G ENSP00000345719.4:n.445-165C>G
ENST00000473604.2:n.555-165C>G
NM_000113.2:c.445-165C>G NP_000104.1:n.445-165C>G
XR_929731.1:n.605-165C>G
XR_929731.3:n.473-165C>G
NM_000113.3:c.445-165C>G MANE Select NP_000104.1:n.445-165C>G
Search 100 bp 5'
Search 100 bp 3'