Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541220A>G , CM000680.2:g.31541220A>G | GRCh38 |
| NC_000018.9:g.29121183A>G , CM000680.1:g.29121183A>G | GRCh37 |
| NC_000018.8:g.27375181A>G | NCBI36 |
| NG_007072.3:g.47979A>G , LRG_397:g.47979A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.1907A>G MANE Select | ENSP00000261590.8:p.His636Arg | |
| ENST00000261590.12:c.1907A>G | ENSP00000261590.8:p.His636Arg | |
| NM_001943.3:c.1907A>G , LRG_397t1:c.1907A>G | NP_001934.2:p.His636Arg | |
| NM_001943.4:c.1907A>G | NP_001934.2:p.His636Arg | |
| XM_024451095.1:c.1373A>G | XP_024306863.1:p.His458Arg | |
| NM_001943.5:c.1907A>G MANE Select | NP_001934.2:p.His636Arg |