Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827275T>C , CM000667.2:g.148827275T>C | GRCh38 |
| NC_000005.9:g.148206838T>C , CM000667.1:g.148206838T>C | GRCh37 |
| NC_000005.8:g.148187031T>C | NCBI36 |
| NG_016421.1:g.5683T>C | |
| NG_016421.2:g.5683T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.444T>C MANE Select | ENSP00000305372.4:p.Asn148= | |
| ENST00000305988.5:c.444T>C | ENSP00000305372.4:p.Asn148= | |
| NM_000024.5:c.444T>C | NP_000015.1:p.Asn148= | |
| NM_000024.6:c.444T>C MANE Select | NP_000015.2:p.Asn148= |