Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585631G>A , CM000665.2:g.98585631G>A | GRCh38 |
| NC_000003.11:g.98304475G>A , CM000665.1:g.98304475G>A | GRCh37 |
| NC_000003.10:g.99787165G>A | NCBI36 |
| NG_015994.1:g.12981C>T | |
| NG_015994.2:g.12981C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000097.7:c.982C>T MANE Select | NP_000088.3:p.Arg328Cys |
| ENST00000647941.2:c.982C>T MANE Select | ENSP00000497326.1:p.Arg328Cys |
| NM_000097.5:c.982C>T | NP_000088.3:p.Arg328Cys |
| ENST00000264193.2:c.982C>T | ENSP00000264193.2:p.Arg328Cys |
| ENST00000510489.1:n.232C>T | |
| XM_005247125.3:c.982C>T | XP_005247182.1:p.Arg328Cys |
| XM_005247125.4:c.982C>T | XP_005247182.1:p.Arg328Cys |
| XR_001740025.2:n.1153C>T | |
| XR_001740026.1:n.1717C>T | |
| XR_001740027.1:n.1257C>T | |
| XR_001740028.1:n.1223C>T |