Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30968872C= , CM000669.2:g.30968872C= | GRCh38 |
| NC_000007.13:g.31008487C= , CM000669.1:g.31008487C= | GRCh37 |
| NC_000007.12:g.30975012C= | NCBI36 |
| NG_021416.1:g.9852C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326139.7:c.96C= MANE Select | ENSP00000320180.2:p.Thr32= | |
| ENST00000326139.6:c.96C= | ENSP00000320180.2:p.Thr32= | |
| ENST00000466427.1:n.323C= | ||
| NM_000823.3:c.96C= | NP_000814.2:p.Thr32= | |
| NM_000823.4:c.96C= MANE Select | NP_000814.2:p.Thr32= |