Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.74457249G= , CM000673.2:g.74457249G= | GRCh38 |
| NC_000011.9:g.74168294G= , CM000673.1:g.74168294G= | GRCh37 |
| NC_000011.8:g.73845942G= | NCBI36 |
| NG_011833.1:g.15307C= , LRG_439:g.15307C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310128.9:c.*3C= MANE Select | ENSP00000310557.4:n.*3C= | |
| ENST00000310128.8:c.*3C= | ENSP00000310557.4:n.*3C= | |
| ENST00000525550.1:c.*3C= | ENSP00000433633.1:n.*3C= | |
| NM_005472.4:c.*3C= , LRG_439t1:c.*3C= | NP_005463.1:n.*3C= | |
| XM_011544713.1:c.*3C= | XP_011543015.1:n.*3C= | |
| XM_011544713.2:c.*3C= | XP_011543015.1:n.*3C= | |
| XM_017017047.1:c.*3C= | XP_016872536.1:n.*3C= | |
| XM_017017048.1:c.*3C= | XP_016872537.1:n.*3C= | |
| XM_017017049.1:c.*3C= | XP_016872538.1:n.*3C= | |
| XM_017017051.2:c.*3C= | XP_016872540.1:n.*3C= | |
| XM_017017052.1:c.*3C= | XP_016872541.1:n.*3C= | |
| NM_005472.5:c.*3C= MANE Select | NP_005463.1:n.*3C= |