Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55156237C>T , CM000681.2:g.55156237C>T | GRCh38 |
| NC_000019.9:g.55667605C>T , CM000681.1:g.55667605C>T | GRCh37 |
| NC_000019.8:g.60359417C>T | NCBI36 |
| NG_007866.2:g.6496G>A , LRG_432:g.6496G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.246G>A MANE Select | ENSP00000341838.5:p.Pro82= | |
| ENST00000665070.1:c.246G>A | ENSP00000499482.1:p.Pro82= | |
| ENST00000344887.9:c.246G>A | ENSP00000341838.5:p.Pro82= | |
| ENST00000585806.5:n.245G>A | ||
| ENST00000586669.5:n.254G>A | ||
| ENST00000587176.5:n.430G>A | ||
| ENST00000587871.1:c.865G>A | ||
| ENST00000588882.1:c.171G>A | ENSP00000466729.1:p.Pro57= | |
| ENST00000590463.1:n.418G>A | ||
| NM_000363.4:c.246G>A , LRG_432t1:c.246G>A | NP_000354.4:p.Pro82= | |
| NM_000363.5:c.246G>A MANE Select | NP_000354.4:p.Pro82= |