Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12833854C>T , CM000686.2:g.12833854C>T | GRCh38 |
| NC_000024.9:g.14945780C>T , CM000686.1:g.14945780C>T | GRCh37 |
| NC_000024.8:g.13455174C>T | NCBI36 |
| NG_008311.1:g.137621C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.5188C>T | ENSP00000498372.1:p.Pro1730Ser | |
| ENST00000338981.7:c.5188C>T MANE Select | ENSP00000342812.3:p.Pro1730Ser | |
| ENST00000426564.6:n.5200C>T | ||
| NM_004654.3:c.5188C>T | NP_004645.2:p.Pro1730Ser | |
| XM_011531469.1:c.5188C>T | XP_011529771.1:p.Pro1730Ser | |
| XM_011531470.1:c.4954C>T | XP_011529772.1:p.Pro1652Ser | |
| XM_017030078.2:c.5203C>T | XP_016885567.1:p.Pro1735Ser | |
| NM_004654.4:c.5188C>T MANE Select | NP_004645.2:p.Pro1730Ser |