Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55151860C>G , CM000681.2:g.55151860C>G | GRCh38 |
| NC_000019.9:g.55663228C>G , CM000681.1:g.55663228C>G | GRCh37 |
| NC_000019.8:g.60355040C>G | NCBI36 |
| NG_007866.2:g.10873G>C , LRG_432:g.10873G>C | |
| NG_011829.2:g.2379G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.607G>C MANE Select | NP_000354.4:p.Gly203Arg |
| ENST00000344887.10:c.607G>C MANE Select | ENSP00000341838.5:p.Gly203Arg |
| NM_000363.4:c.607G>C , LRG_432t1:c.607G>C | NP_000354.4:p.Gly203Arg |
| ENST00000344887.9:c.607G>C | ENSP00000341838.5:p.Gly203Arg |
| ENST00000585806.5:n.606G>C | |
| ENST00000588882.1:c.532G>C | ENSP00000466729.1:p.Gly178Arg |
| ENST00000589864.1:n.435G>C | |
| ENST00000665070.1:c.640G>C | ENSP00000499482.1:p.Gly214Arg |