Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240873239T= , CM000664.2:g.240873239T= | GRCh38 |
| NC_000002.11:g.241812656T= , CM000664.1:g.241812656T= | GRCh37 |
| NC_000002.10:g.241461329T= | NCBI36 |
| NG_008005.1:g.9495T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.595+190T= MANE Select | ENSP00000302620.3:n.595+190T= | |
| ENST00000307503.3:c.595+190T= | ENSP00000302620.3:n.595+190T= | |
| ENST00000472436.1:n.805T= | ||
| ENST00000476698.1:n.332+190T= | ||
| NM_000030.2:c.595+190T= | NP_000021.1:n.595+190T= | |
| NM_000030.3:c.595+190T= MANE Select | NP_000021.1:n.595+190T= |