Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940395G>T , CM000678.2:g.67940395G>T | GRCh38 |
| NC_000016.9:g.67974298G>T , CM000678.1:g.67974298G>T | GRCh37 |
| NC_000016.8:g.66531799G>T | NCBI36 |
| NG_009778.1:g.8718C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.832C>A MANE Select | ENSP00000264005.5:p.Pro278Thr | |
| ENST00000264005.9:c.832C>A | ENSP00000264005.5:p.Pro278Thr | |
| ENST00000570369.5:c.156-321C>A | ||
| ENST00000570980.1:c.616C>A | ENSP00000464651.1:p.Pro206Thr | |
| ENST00000573538.5:c.570C>A | ENSP00000463220.1:n.570C>A | |
| NM_000229.1:c.832C>A | NP_000220.1:p.Pro278Thr | |
| NM_000229.2:c.832C>A MANE Select | NP_000220.1:p.Pro278Thr |