Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6620205T= , CM000671.2:g.6620205T= | GRCh38 |
| NC_000009.11:g.6620205T= , CM000671.1:g.6620205T= | GRCh37 |
| NC_000009.10:g.6610205T= | NCBI36 |
| NG_016397.1:g.30488A= , LRG_643:g.30488A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000170.3:c.449A= MANE Select | NP_000161.2:p.Asn150= |
| ENST00000321612.8:c.449A= MANE Select | ENSP00000370737.4:p.Asn150= |
| NM_000170.2:c.449A= , LRG_643t1:c.449A= | NP_000161.2:p.Asn150= |
| ENST00000321612.6:c.449A= | ENSP00000370737.3:p.Asn150= |
| ENST00000639020.1:c.44A= | ENSP00000491392.1:p.Asn15= |
| ENST00000639364.1:n.149A= | |
| ENST00000639840.1:c.155A= | ENSP00000491161.1:p.Asn52= |
| ENST00000639954.1:n.179-9849A= | |
| ENST00000640592.1:n.332A= |