Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868900A= , CM000664.2:g.240868900A= | GRCh38 |
| NC_000002.11:g.241808317A= , CM000664.1:g.241808317A= | GRCh37 |
| NC_000002.10:g.241456990A= | NCBI36 |
| NG_008005.1:g.5156A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.35A= MANE Select | ENSP00000302620.3:p.Lys12= | |
| ENST00000307503.3:c.35A= | ENSP00000302620.3:p.Lys12= | |
| ENST00000472436.1:n.55A= | ||
| NM_000030.2:c.35A= | NP_000021.1:p.Lys12= | |
| XR_924060.1:n.405+1333T= | ||
| NM_000030.3:c.35A= MANE Select | NP_000021.1:p.Lys12= |