Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67435830C= , CM000678.2:g.67435830C= | GRCh38 |
| NC_000016.9:g.67469733C= , CM000678.1:g.67469733C= | GRCh37 |
| NC_000016.8:g.66027234C= | NCBI36 |
| NG_016549.1:g.9698C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000196.4:c.468C= MANE Select | NP_000187.3:p.Thr156= |
| ENST00000326152.6:c.468C= MANE Select | ENSP00000316786.5:p.Thr156= |
| NM_000196.3:c.468C= | NP_000187.3:p.Thr156= |
| ENST00000326152.5:c.468C= | ENSP00000316786.5:p.Thr156= |
| ENST00000566606.1:c.446C= | ENSP00000473429.1:n.446C= |
| ENST00000567684.2:n.331C= |