Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.42249493G>A , CM000681.2:g.42249493G>A | GRCh38 |
| NC_000019.9:g.42753645G>A , CM000681.1:g.42753645G>A | GRCh37 |
| NC_000019.8:g.47445485G>A | NCBI36 |
| NG_042802.1:g.10672C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222329.9:c.619C>T MANE Select | ENSP00000222329.3:p.Arg207Ter | |
| ENST00000222329.8:c.619C>T | ENSP00000222329.3:p.Arg207Ter | |
| ENST00000440177.6:c.394C>T | ENSP00000388173.2:p.Arg132Ter | |
| ENST00000594664.1:c.22+5485C>T | ENSP00000470087.1:n.22+5485C>T | |
| NM_001301035.1:c.394C>T | NP_001287964.1:p.Arg132Ter | |
| NM_001308402.1:c.394C>T | NP_001295331.1:p.Arg132Ter | |
| NM_001312656.1:c.394C>T | NP_001299585.1:p.Arg132Ter | |
| NM_006494.3:c.619C>T | NP_006485.2:p.Arg207Ter | |
| XM_011526612.1:c.394C>T | XP_011524914.1:p.Arg132Ter | |
| XM_011526613.1:c.394C>T | XP_011524915.1:p.Arg132Ter | |
| XM_017026468.1:c.394C>T | XP_016881957.1:p.Arg132Ter | |
| XM_017026469.1:c.394C>T | XP_016881958.1:p.Arg132Ter | |
| NM_006494.4:c.619C>T MANE Select | NP_006485.2:p.Arg207Ter | |
| NM_001308402.2:c.394C>T | NP_001295331.1:p.Arg132Ter | |
| NM_001312656.2:c.394C>T | NP_001299585.1:p.Arg132Ter | |
| NM_001301035.2:c.394C>T | NP_001287964.1:p.Arg132Ter |