Canonical Allele Identifier: CA1880971322
Gene: TOR1A HGNC NCBI

Linked Data

dbSNP Id: rs1588214668

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129813955G>C , CM000671.2:g.129813955G>C GRCh38
NC_000009.11:g.132576234G>C , CM000671.1:g.132576234G>C GRCh37
NC_000009.10:g.131616055G>C NCBI36
NG_008049.1:g.15208C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.*17C>G MANE Select ENSP00000345719.4:n.*17C>G
ENST00000651202.1:c.*284C>G ENSP00000498222.1:n.*284C>G
ENST00000351698.4:c.*17C>G ENSP00000345719.4:n.*17C>G
ENST00000474192.1:n.600C>G
NM_000113.2:c.*17C>G NP_000104.1:n.*17C>G
XR_929731.3:n.1211C>G
NM_000113.3:c.*17C>G MANE Select NP_000104.1:n.*17C>G