Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2250667C= , CM000681.2:g.2250667C= | GRCh38 |
| NC_000019.9:g.2250666C= , CM000681.1:g.2250666C= | GRCh37 |
| NC_000019.8:g.2201666C= | NCBI36 |
| NG_012190.1:g.6554C= | |
| NG_032853.1:g.10757G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000479.5:c.571C= (AMH) MANE Select | NP_000470.3:p.Arg191= |
| ENST00000221496.5:c.571C= (AMH) MANE Select | ENSP00000221496.2:p.Arg191= |
| NM_000479.3:c.571C= (AMH) | NP_000470.2:p.Arg191= |
| NM_000479.4:c.571C= (AMH) | NP_000470.2:p.Arg191= |
| NR_036207.1:n.29C= (MIR4321) | |
| ENST00000221496.4:c.571C= (AMH) | ENSP00000221496.2:p.Arg191= |
| ENST00000589313.2:n.924C= (AMH) | |
| ENST00000592877.1:n.452C= (AMH) |