Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780516A= , CM000672.2:g.94780516A= | GRCh38 |
| NC_000010.10:g.96540273A= , CM000672.1:g.96540273A= | GRCh37 |
| NC_000010.9:g.96530263A= | NCBI36 |
| NG_008384.2:g.22811A= | |
| NG_008384.3:g.22836A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.9:c.499A= MANE Select | ENSP00000360372.3:p.Thr167= | |
| ENST00000645461.1:n.1552A= | ||
| ENST00000371321.7:c.499A= | ENSP00000360372.3:p.Thr167= | |
| ENST00000464755.1:c.1262A= | ENSP00000483243.1:n.1262A= | |
| NM_000769.2:c.499A= | NP_000760.1:p.Thr167= | |
| NM_000769.4:c.499A= MANE Select | NP_000760.1:p.Thr167= |