Linked Data
MyVariant Identifiers:
chr12:g.122284771T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121846865T>A , CM000674.2:g.121846865T>A | GRCh38 |
| NC_000012.11:g.122284771T>A , CM000674.1:g.122284771T>A | GRCh37 |
| NC_000012.10:g.120769154T>A | NCBI36 |
| NG_016461.1:g.46747A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289004.8:c.828A>T MANE Select | ENSP00000289004.4:p.Thr276= | |
| ENST00000543163.5:c.711A>T | ENSP00000441677.1:p.Thr237= | |
| NM_001171993.1:c.711A>T | NP_001165464.1:p.Thr237= | |
| NM_002150.2:c.828A>T | NP_002141.1:p.Thr276= | |
| NM_002150.3:c.828A>T MANE Select | NP_002141.2:p.Thr276= | |
| NM_001171993.2:c.711A>T | NP_001165464.1:p.Thr237= |