Linked Data
MyVariant Identifiers:
chr19:g.48922981C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48419724C>T , CM000681.2:g.48419724C>T | GRCh38 |
| NC_000019.9:g.48922981C>T , CM000681.1:g.48922981C>T | GRCh37 |
| NC_000019.8:g.53614793C>T | NCBI36 |
| NG_052829.1:g.29850C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263269.4:c.2001C>T MANE Select | ENSP00000263269.2:p.Val667= | |
| ENST00000263269.3:c.2001C>T | ENSP00000263269.2:p.Val667= | |
| NM_000836.2:c.2001C>T | NP_000827.2:p.Val667= | |
| XM_011526872.1:c.2001C>T | XP_011525174.1:p.Val667= | |
| NM_000836.4:c.2001C>T MANE Select | NP_000827.2:p.Val667= |