Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812370C>T , CM000672.2:g.110812370C>T | GRCh38 |
| NC_000010.10:g.112572128C>T , CM000672.1:g.112572128C>T | GRCh37 |
| NC_000010.9:g.112562118C>T | NCBI36 |
| NG_021177.1:g.172974C>T , LRG_382:g.172974C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.1973C>T MANE Select | ENSP00000358532.3:p.Ser658Phe | |
| ENST00000369519.3:c.1973C>T | ENSP00000358532.3:p.Ser658Phe | |
| NM_001134363.2:c.1973C>T | NP_001127835.2:p.Ser658Phe | |
| XM_011539697.1:c.1589C>T | XP_011537999.1:p.Ser530Phe | |
| XM_017016103.2:c.1808C>T | XP_016871592.1:p.Ser603Phe | |
| XM_017016104.2:c.1589C>T | XP_016871593.1:p.Ser530Phe | |
| NM_001134363.3:c.1973C>T MANE Select | NP_001127835.2:p.Ser658Phe |