Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965718G>C , CM000670.2:g.37965718G>C | GRCh38 |
| NC_000008.10:g.37823236G>C , CM000670.1:g.37823236G>C | GRCh37 |
| NC_000008.9:g.37942393G>C | NCBI36 |
| NG_011936.1:g.5949C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.752C>G MANE Select | NP_000016.1:p.Pro251Arg |
| ENST00000345060.5:c.752C>G MANE Select | ENSP00000343782.3:p.Pro251Arg |
| NM_000025.2:c.752C>G | NP_000016.1:p.Pro251Arg |
| ENST00000345060.4:c.752C>G | ENSP00000343782.3:p.Pro251Arg |
| ENST00000520341.1:n.27C>G | |
| ENST00000520341.2:n.880C>G | |
| ENST00000614635.1:c.752C>G | ENSP00000480325.1:p.Pro251Arg |
| ENST00000647937.1:c.236C>G | ENSP00000497740.1:p.Pro79Arg |