Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228158026C>T , CM000663.2:g.228158026C>T | GRCh38 |
| NC_000001.10:g.228345727C>T , CM000663.1:g.228345727C>T | GRCh37 |
| NC_000001.9:g.226412350C>T | NCBI36 |
| NG_011838.1:g.13175C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020435.4:c.268C>T MANE Select | NP_065168.2:p.Pro90Ser |
| ENST00000366714.3:c.268C>T MANE Select | ENSP00000355675.2:p.Pro90Ser |
| NM_020435.3:c.268C>T | NP_065168.2:p.Pro90Ser |
| ENST00000366714.2:c.268C>T | ENSP00000355675.2:p.Pro90Ser |