Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135809062G>A , CM000664.2:g.135809062G>A | GRCh38 |
| NC_000002.11:g.136566632G>A , CM000664.1:g.136566632G>A | GRCh37 |
| NC_000002.10:g.136283102G>A | NCBI36 |
| NG_008104.2:g.51108C>T , LRG_338:g.51108C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002299.4:c.3285C>T MANE Select | NP_002290.2:p.His1095= |
| ENST00000264162.7:c.3285C>T MANE Select | ENSP00000264162.2:p.His1095= |
| NM_002299.2:c.3285C>T , LRG_338t1:c.3285C>T | NP_002290.2:p.His1095= |
| NM_002299.3:c.3285C>T | NP_002290.2:p.His1095= |
| ENST00000264162.6:c.3285C>T | ENSP00000264162.2:p.His1095= |
| ENST00000452974.1:c.1581C>T | ENSP00000391231.1:p.His527= |
| XM_017004088.2:c.3285C>T | XP_016859577.1:p.His1095= |