Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.26336611G= , CM000674.2:g.26336611G= | GRCh38 |
| NC_000012.11:g.26489544G= , CM000674.1:g.26489544G= | GRCh37 |
| NC_000012.10:g.26380811G= | NCBI36 |
| NG_042142.1:g.501588C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381340.8:c.*2786C= MANE Select | ENSP00000370744.3:n.*2786C= | |
| ENST00000381340.7:c.*2786C= | ENSP00000370744.3:n.*2786C= | |
| NM_002223.2:c.*2786C= | NP_002214.2:n.*2786C= | |
| NM_002223.3:c.*2786C= | NP_002214.2:n.*2786C= | |
| XM_011520645.1:c.*2786C= | XP_011518947.1:n.*2786C= | |
| XM_011520646.1:c.*2786C= | XP_011518948.1:n.*2786C= | |
| XM_017019266.1:c.*2786C= | XP_016874755.1:n.*2786C= | |
| NM_002223.4:c.*2786C= MANE Select | NP_002214.2:n.*2786C= |