gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.235766122G>C , CM000663.2:g.235766122G>C | GRCh38 |
| NC_000001.10:g.235929422G>C , CM000663.1:g.235929422G>C | GRCh37 |
| NC_000001.9:g.233996045G>C | NCBI36 |
| NG_007397.1:g.122519C>G , LRG_143:g.122519C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461526.2:c.753C>G | ENSP00000513165.1:p.Tyr251Ter | |
| ENST00000697178.1:c.*1502C>G | ENSP00000513163.1:n.*1502C>G | |
| ENST00000697180.1:c.583C>G | ||
| ENST00000697241.1:c.510C>G | ENSP00000513206.1:p.Tyr170Ter | |
| ENST00000389793.7:c.6078C>G MANE Select | ENSP00000374443.2:p.Tyr2026Ter | |
| ENST00000389793.6:c.6078C>G | ENSP00000374443.2:p.Tyr2026Ter | |
| ENST00000389794.7:c.*1502C>G | ENSP00000374444.4:n.*1502C>G | |
| ENST00000489585.5:n.6512+117C>G | ||
| NM_000081.3:c.6078C>G , LRG_143t1:c.6078C>G | NP_000072.2:p.Tyr2026Ter | |
| NM_001301365.1:c.6078C>G , LRG_143t2:c.6078C>G | NP_001288294.1:p.Tyr2026Ter | |
| XM_011544031.1:c.6078C>G | XP_011542333.1:p.Tyr2026Ter | |
| XM_011544032.1:c.6078C>G | XP_011542334.1:p.Tyr2026Ter | |
| XM_011544033.1:c.6078C>G | XP_011542335.1:p.Tyr2026Ter | |
| XM_011544034.1:c.5940C>G | XP_011542336.1:p.Tyr1980Ter | |
| XM_011544035.1:c.6078C>G | XP_011542337.1:p.Tyr2026Ter | |
| XM_011544036.1:c.3741C>G | XP_011542338.1:p.Tyr1247Ter | |
| XM_011544037.1:c.6078C>G | XP_011542339.1:p.Tyr2026Ter | |
| XM_011544038.1:c.6078C>G | XP_011542340.1:p.Tyr2026Ter | |
| XM_011544039.1:c.6078C>G | XP_011542341.1:p.Tyr2026Ter | |
| XM_011544040.1:c.5987C>G | XP_011542342.1:p.Thr1996Arg | |
| XM_011544033.2:c.6078C>G | XP_011542335.1:p.Tyr2026Ter | |
| XM_011544035.2:c.6078C>G | XP_011542337.1:p.Tyr2026Ter | |
| XM_011544036.2:c.3741C>G | XP_011542338.1:p.Tyr1247Ter | |
| XM_011544037.2:c.6078C>G | XP_011542339.1:p.Tyr2026Ter | |
| XM_011544039.2:c.6078C>G | XP_011542341.1:p.Tyr2026Ter | |
| XM_017000150.1:c.6078C>G | XP_016855639.1:p.Tyr2026Ter | |
| XM_017000151.1:c.5849C>G | XP_016855640.1:p.Thr1950Arg | |
| XR_001736946.2:n.6260C>G | ||
| XR_001736947.1:n.6260C>G | ||
| XR_001736948.1:n.6260C>G | ||
| XR_002959252.1:n.6169C>G | ||
| NM_000081.4:c.6078C>G MANE Select | NP_000072.2:p.Tyr2026Ter |