Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849600C>G , CM000681.2:g.35849600C>G | GRCh38 |
| NC_000019.9:g.36340502C>G , CM000681.1:g.36340502C>G | GRCh37 |
| NC_000019.8:g.41032342C>G | NCBI36 |
| NG_013356.2:g.24688G>C , LRG_693:g.24688G>C | |
| NG_051206.1:g.2966C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.662G>C MANE Select | ENSP00000368190.4:p.Ser221Thr | |
| ENST00000353632.6:c.662G>C | ENSP00000343634.5:p.Ser221Thr | |
| ENST00000378910.9:c.662G>C | ENSP00000368190.4:p.Ser221Thr | |
| NM_004646.3:c.662G>C , LRG_693t1:c.662G>C | NP_004637.1:p.Ser221Thr | |
| NM_004646.4:c.662G>C MANE Select | NP_004637.1:p.Ser221Thr |