Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35826642G>A , CM000681.2:g.35826642G>A | GRCh38 |
| NC_000019.9:g.36317544G>A , CM000681.1:g.36317544G>A | GRCh37 |
| NC_000019.8:g.41009384G>A | NCBI36 |
| NG_013356.2:g.47646C>T , LRG_693:g.47646C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.3598C>T MANE Select | NP_004637.1:p.Pro1200Ser |
| ENST00000378910.10:c.3598C>T MANE Select | ENSP00000368190.4:p.Pro1200Ser |
| NM_004646.3:c.3598C>T , LRG_693t1:c.3598C>T | NP_004637.1:p.Pro1200Ser |
| ENST00000353632.6:c.3478C>T | ENSP00000343634.5:p.Pro1160Ser |
| ENST00000378910.9:c.3598C>T | ENSP00000368190.4:p.Pro1200Ser |