Linked Data
MyVariant Identifiers:
chr13:g.28498799C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924662C>T , CM000675.2:g.27924662C>T | GRCh38 |
| NC_000013.10:g.28498799C>T , CM000675.1:g.28498799C>T | GRCh37 |
| NC_000013.9:g.27396799C>T | NCBI36 |
| NG_008183.1:g.9632C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.813C>T MANE Select | ENSP00000370421.4:p.Pro271= | |
| ENST00000381033.4:c.813C>T | ENSP00000370421.4:p.Pro271= | |
| NM_000209.3:c.813C>T | NP_000200.1:p.Pro271= | |
| NM_000209.4:c.813C>T MANE Select | NP_000200.1:p.Pro271= |