Canonical Allele Identifier: CA2692045227
Gene: TOR1A HGNC NCBI

Linked Data

dbSNP Id: rs1313515668

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129813537T>C , CM000671.2:g.129813537T>C GRCh38
NC_000009.11:g.132575816T>C , CM000671.1:g.132575816T>C GRCh37
NC_000009.10:g.131615637T>C NCBI36
NG_008049.1:g.15626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.*435A>G MANE Select ENSP00000345719.4:n.*435A>G
ENST00000651202.1:c.*702A>G ENSP00000498222.1:n.*702A>G
ENST00000351698.4:c.*435A>G ENSP00000345719.4:n.*435A>G
NM_000113.2:c.*435A>G NP_000104.1:n.*435A>G
XR_929731.3:n.1629A>G
NM_000113.3:c.*435A>G MANE Select NP_000104.1:n.*435A>G