Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162273913C>A , CM000664.2:g.162273913C>A | GRCh38 |
| NC_000002.11:g.163130423C>A , CM000664.1:g.163130423C>A | GRCh37 |
| NC_000002.10:g.162838669C>A | NCBI36 |
| NG_011495.1:g.49617G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697291.1:c.*1933G>T | ENSP00000513228.1:n.*1933G>T | |
| ENST00000648433.1:c.2219G>T | ENSP00000496816.1:p.Arg740Leu | |
| ENST00000649554.1:n.1946G>T | ||
| ENST00000649979.2:c.2336G>T MANE Select | ENSP00000497271.1:p.Arg779Leu | |
| ENST00000679938.1:c.2024G>T | ENSP00000505518.1:p.Arg675Leu | |
| ENST00000263642.2:c.2336G>T | ENSP00000263642.2:p.Arg779Leu | |
| NM_022168.3:c.2336G>T | NP_071451.2:p.Arg779Leu | |
| XM_011511628.1:c.1619G>T | XP_011509930.1:p.Arg540Leu | |
| NM_022168.4:c.2336G>T MANE Select | NP_071451.2:p.Arg779Leu |