Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868892C= , CM000664.2:g.240868892C= | GRCh38 |
| NC_000002.11:g.241808309C= , CM000664.1:g.241808309C= | GRCh37 |
| NC_000002.10:g.241456982C= | NCBI36 |
| NG_008005.1:g.5148C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.27C= MANE Select | ENSP00000302620.3:p.Thr9= | |
| ENST00000307503.3:c.27C= | ENSP00000302620.3:p.Thr9= | |
| ENST00000472436.1:n.47C= | ||
| NM_000030.2:c.27C= | NP_000021.1:p.Thr9= | |
| XR_924060.1:n.405+1341G= | ||
| NM_000030.3:c.27C= MANE Select | NP_000021.1:p.Thr9= |