Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.10760194G>T , CM000673.2:g.10760194G>T | GRCh38 |
| NC_000011.9:g.10781741G>T , CM000673.1:g.10781741G>T | GRCh37 |
| NC_000011.8:g.10738317G>T | NCBI36 |
| NG_051671.1:g.14208G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361367.7:c.614G>T MANE Select | ENSP00000355013.2:p.Gly205Val | |
| ENST00000361367.6:c.614G>T | ENSP00000355013.2:p.Gly205Val | |
| ENST00000524523.1:c.575G>T | ENSP00000431458.1:p.Gly192Val | |
| NM_014633.4:c.614G>T | NP_055448.1:p.Gly205Val | |
| NM_001346279.1:c.614G>T | NP_001333208.1:p.Gly205Val | |
| NM_014633.5:c.614G>T MANE Select | NP_055448.1:p.Gly205Val | |
| NM_001346279.2:c.614G>T | NP_001333208.1:p.Gly205Val |