Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713251G>C , CM000681.2:g.6713251G>C | GRCh38 |
| NC_000019.9:g.6713262G>C , CM000681.1:g.6713262G>C | GRCh37 |
| NC_000019.8:g.6664262G>C | NCBI36 |
| NG_009557.1:g.12401C>G , LRG_27:g.12401C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695652.1:c.818C>G | ENSP00000512083.1:p.Pro273Arg | |
| ENST00000695654.1:c.65C>G | ENSP00000512085.1:p.Pro22Arg | |
| ENST00000695692.1:n.265C>G | ||
| ENST00000245907.11:c.941C>G MANE Select | ENSP00000245907.4:p.Pro314Arg | |
| ENST00000245907.10:c.941C>G | ENSP00000245907.4:p.Pro314Arg | |
| ENST00000594270.5:n.65C>G | ||
| ENST00000595577.1:n.445C>G | ||
| ENST00000597442.5:n.191C>G | ||
| NM_000064.3:c.941C>G | NP_000055.2:p.Pro314Arg | |
| NM_000064.4:c.941C>G MANE Select | NP_000055.2:p.Pro314Arg |