Linked Data
MyVariant Identifiers:
chr16:g.31004520A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30993199A>C , CM000678.2:g.30993199A>C | GRCh38 |
| NC_000016.9:g.31004520A>C , CM000678.1:g.31004520A>C | GRCh37 |
| NC_000016.8:g.30912021A>C | NCBI36 |
| NG_041829.1:g.22310T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215095.11:c.717T>G MANE Select | ENSP00000215095.5:p.Ser239= | |
| ENST00000565419.2:c.717T>G | ENSP00000455899.1:p.Ser239= | |
| ENST00000215095.9:c.717T>G | ENSP00000215095.5:p.Ser239= | |
| ENST00000565419.1:c.717T>G | ENSP00000455899.1:p.Ser239= | |
| ENST00000569638.5:c.465T>G | ENSP00000457067.1:p.Ser155= | |
| NM_052874.4:c.717T>G | NP_443106.1:p.Ser239= | |
| XM_017022893.1:c.699T>G | XP_016878382.1:p.Ser233= | |
| NM_052874.5:c.717T>G MANE Select | NP_443106.1:p.Ser239= |