Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869309T= , CM000664.2:g.240869309T= | GRCh38 |
| NC_000002.11:g.241808726T= , CM000664.1:g.241808726T= | GRCh37 |
| NC_000002.10:g.241457399T= | NCBI36 |
| NG_008005.1:g.5565T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.305T= MANE Select | ENSP00000302620.3:p.Val102= | |
| ENST00000307503.3:c.305T= | ENSP00000302620.3:p.Val102= | |
| ENST00000472436.1:n.325T= | ||
| NM_000030.2:c.305T= | NP_000021.1:p.Val102= | |
| XR_924060.1:n.405+924A= | ||
| NM_000030.3:c.305T= MANE Select | NP_000021.1:p.Val102= |