Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.65982192G= , CM000669.2:g.65982192G= | GRCh38 |
| NC_000007.13:g.65447179G= , CM000669.1:g.65447179G= | GRCh37 |
| NC_000007.12:g.65084614G= | NCBI36 |
| NG_016197.1:g.5123C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304895.9:c.-9C= MANE Select | ENSP00000302728.4:n.-9C= | |
| ENST00000304895.8:c.-9C= | ENSP00000302728.4:n.-9C= | |
| ENST00000421103.5:c.-9C= | ENSP00000391390.1:n.-9C= | |
| ENST00000430730.5:c.-9C= | ENSP00000411859.1:n.-9C= | |
| ENST00000446111.1:c.-9C= | ENSP00000416793.1:n.-9C= | |
| ENST00000447929.5:c.-9C= | ENSP00000411262.1:n.-9C= | |
| NM_000181.3:c.-9C= | NP_000172.2:n.-9C= | |
| NM_001284290.1:c.-9C= | NP_001271219.1:n.-9C= | |
| NM_001293104.1:c.-394C= | NP_001280033.1:n.-394C= | |
| NM_001293105.1:c.-338C= | NP_001280034.1:n.-338C= | |
| NR_120531.1:n.123C= | ||
| XM_005250297.3:c.-9C= | XP_005250354.1:n.-9C= | |
| XM_011516113.1:c.-338C= | XP_011514415.1:n.-338C= | |
| XR_927461.1:n.118C= | ||
| XM_005250297.4:c.-9C= | XP_005250354.1:n.-9C= | |
| XM_011516114.2:c.-694C= | XP_011514416.1:n.-694C= | |
| XM_017012091.1:c.-338C= | XP_016867580.1:n.-338C= | |
| XM_017012092.1:c.-394C= | XP_016867581.1:n.-394C= | |
| XM_017012093.2:c.-694C= | XP_016867582.1:n.-694C= | |
| XR_001744658.2:n.37C= | ||
| XR_001744659.2:n.37C= | ||
| XR_001744660.2:n.37C= | ||
| XR_001744661.2:n.37C= | ||
| XR_927461.3:n.37C= | ||
| NM_000181.4:c.-9C= MANE Select | NP_000172.2:n.-9C= | |
| NM_001284290.2:c.-9C= | NP_001271219.1:n.-9C= | |
| NM_001293104.2:c.-394C= | NP_001280033.1:n.-394C= | |
| NM_001293105.2:c.-338C= | NP_001280034.1:n.-338C= | |
| NR_120531.2:n.22C= |