Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541990A= , CM000671.2:g.98541990A= | GRCh38 |
| NC_000009.11:g.101304272A= , CM000671.1:g.101304272A= | GRCh37 |
| NC_000009.10:g.100344093A= | NCBI36 |
| NG_016426.1:g.172208T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.513T= MANE Select | ENSP00000259455.2:p.Tyr171= | |
| ENST00000637410.1:n.291T= | ||
| ENST00000637717.1:c.129T= | ENSP00000490789.1:p.Tyr43= | |
| ENST00000259455.3:c.513T= | ENSP00000259455.2:p.Tyr171= | |
| ENST00000477471.1:n.300T= | ||
| ENST00000634227.1:n.287T= | ||
| NM_005458.7:c.513T= | NP_005449.5:p.Tyr171= | |
| XM_017015331.2:c.219T= | XP_016870820.1:p.Tyr73= | |
| NM_005458.8:c.513T= MANE Select | NP_005449.5:p.Tyr171= |