Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436797T= , CM000678.2:g.67436797T= | GRCh38 |
| NC_000016.9:g.67470700T= , CM000678.1:g.67470700T= | GRCh37 |
| NC_000016.8:g.66028201T= | NCBI36 |
| NG_011482.1:g.49390A= | |
| NG_016549.1:g.10665T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000196.4:c.1012T= MANE Select | NP_000187.3:p.Tyr338= |
| ENST00000326152.6:c.1012T= MANE Select | ENSP00000316786.5:p.Tyr338= |
| NM_000196.3:c.1012T= | NP_000187.3:p.Tyr338= |
| ENST00000326152.5:c.1012T= | ENSP00000316786.5:p.Tyr338= |