Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81670875T>G , CM000665.2:g.81670875T>G | GRCh38 |
| NC_000003.11:g.81720026T>G , CM000665.1:g.81720026T>G | GRCh37 |
| NC_000003.10:g.81802716T>G | NCBI36 |
| NG_011810.1:g.95926A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.392A>C MANE Select | ENSP00000410833.2:p.Asn131Thr | |
| ENST00000429644.6:c.392A>C | ENSP00000410833.2:p.Asn131Thr | |
| ENST00000477426.1:n.108A>C | ||
| ENST00000489715.1:c.269A>C | ENSP00000419638.1:p.Asn90Thr | |
| NM_000158.3:c.392A>C | NP_000149.3:p.Asn131Thr | |
| NM_000158.4:c.392A>C MANE Select | NP_000149.4:p.Asn131Thr |