Linked Data
ClinVar Variation Id:
411270
dbSNP Id:
rs746607455
gnomAD v2:
9-135776113-C-G
gnomAD v3:
9-132900726-C-G
gnomAD v4:
9-132900726-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132900726C>G , CM000671.2:g.132900726C>G | GRCh38 |
| NC_000009.11:g.135776113C>G , CM000671.1:g.135776113C>G | GRCh37 |
| NC_000009.10:g.134765934C>G | NCBI36 |
| NG_012386.1:g.48908G>C , LRG_486:g.48908G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.2611G>C | ENSP00000496126.2:p.Asp871His | |
| ENST00000490179.4:c.2614G>C | ENSP00000495533.2:p.Asp872His | |
| ENST00000642261.2:c.*393G>C | ENSP00000494743.2:n.*393G>C | |
| ENST00000643275.2:c.*554G>C | ENSP00000495598.2:n.*554G>C | |
| ENST00000643362.2:c.2227G>C | ENSP00000496398.2:p.Asp743His | |
| ENST00000643625.2:c.*356G>C | ENSP00000495546.2:n.*356G>C | |
| ENST00000643691.2:c.2251G>C | ENSP00000494916.2:p.Asp751His | |
| ENST00000644184.2:c.2572G>C | ENSP00000495428.2:p.Asp858His | |
| ENST00000645129.2:c.2458G>C | ENSP00000493639.2:p.Asp820His | |
| ENST00000646440.2:c.2614G>C | ENSP00000495830.2:p.Asp872His | |
| ENST00000298552.9:c.2614G>C MANE Select | ENSP00000298552.3:p.Asp872His | |
| ENST00000642261.1:c.674G>C | ||
| ENST00000642617.1:c.2611G>C | ENSP00000493773.1:p.Asp871His | |
| ENST00000642627.1:c.2596G>C | ENSP00000496772.1:p.Asp866His | |
| ENST00000642811.1:c.*2384G>C | ENSP00000495554.1:n.*2384G>C | |
| ENST00000643072.1:c.2461G>C | ENSP00000496691.1:p.Asp821His | |
| ENST00000643275.1:c.1088G>C | ENSP00000495598.1:n.1088G>C | |
| ENST00000643583.1:c.2599G>C | ENSP00000494685.1:p.Asp867His | |
| ENST00000643625.1:c.491G>C | ENSP00000495546.1:n.491G>C | |
| ENST00000643875.1:c.2614G>C | ENSP00000495158.1:p.Asp872His | |
| ENST00000644097.1:c.2611G>C | ENSP00000494682.1:p.Asp871His | |
| ENST00000644184.1:c.1309G>C | ENSP00000495428.1:p.Asp437His | |
| ENST00000644255.1:c.*2381G>C | ENSP00000493608.1:n.*2381G>C | |
| ENST00000644319.1:n.2989G>C | ||
| ENST00000644786.1:n.273G>C | ||
| ENST00000644882.1:n.1527G>C | ||
| ENST00000645901.1:n.3465G>C | ||
| ENST00000646391.1:c.*2384G>C | ENSP00000494104.1:n.*2384G>C | |
| ENST00000646625.1:c.2614G>C | ENSP00000496263.1:p.Asp872His | |
| ENST00000647262.1:n.1579G>C | ||
| ENST00000647279.1:c.*1853G>C | ENSP00000494502.1:n.*1853G>C | |
| ENST00000647506.1:n.3490G>C | ||
| ENST00000647534.1:n.1678G>C | ||
| ENST00000298552.7:c.2614G>C | ENSP00000298552.3:p.Asp872His | |
| ENST00000440111.6:c.2614G>C | ENSP00000394524.2:p.Asp872His | |
| ENST00000545250.5:c.2461G>C | ENSP00000444017.1:p.Asp821His | |
| NM_000368.4:c.2614G>C , LRG_486t1:c.2614G>C | NP_000359.1:p.Asp872His | |
| NM_001162426.1:c.2611G>C | NP_001155898.1:p.Asp871His | |
| NM_001162427.1:c.2461G>C | NP_001155899.1:p.Asp821His | |
| XM_005272211.1:c.2614G>C | XP_005272268.1:p.Asp872His | |
| XM_006717271.1:c.2614G>C | XP_006717334.1:p.Asp872His | |
| XM_011518979.1:c.2614G>C | XP_011517281.1:p.Asp872His | |
| NM_001362177.1:c.2251G>C | NP_001349106.1:p.Asp751His | |
| XM_011518979.2:c.2614G>C | XP_011517281.1:p.Asp872His | |
| XM_017015096.1:c.2614G>C | XP_016870585.1:p.Asp872His | |
| XM_017015097.1:c.2614G>C | XP_016870586.1:p.Asp872His | |
| XM_017015098.1:c.2611G>C | XP_016870587.1:p.Asp871His | |
| XM_017015100.1:c.2251G>C | XP_016870589.1:p.Asp751His | |
| XM_017015101.1:c.2248G>C | XP_016870590.1:p.Asp750His | |
| NM_000368.5:c.2614G>C MANE Select | NP_000359.1:p.Asp872His | |
| NM_001162426.2:c.2611G>C | NP_001155898.1:p.Asp871His | |
| NM_001162427.2:c.2461G>C | NP_001155899.1:p.Asp821His | |
| NM_001362177.2:c.2251G>C | NP_001349106.1:p.Asp751His |