Linked Data
dbSNP Id:
rs772046185
ExAC:
22:50967929 C / A
gnomAD v2:
22-50967929-C-A
gnomAD v4:
22-50529500-C-A
COSMIC:
COSM6095511
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50529500C>A , CM000684.2:g.50529500C>A | GRCh38 |
| NC_000022.10:g.50967929C>A , CM000684.1:g.50967929C>A | GRCh37 |
| NC_000022.9:g.49314795C>A | NCBI36 |
| NG_011860.1:g.5586G>T , LRG_727:g.5586G>T | |
| NG_016235.1:g.1940G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252029.8:c.210G>T MANE Select | ENSP00000252029.3:p.Gln70His | |
| ENST00000395680.6:c.210G>T | ENSP00000379037.1:p.Gln70His | |
| ENST00000395681.6:c.210G>T | ENSP00000379038.1:p.Gln70His | |
| ENST00000650719.1:c.210G>T | ENSP00000498276.1:p.Gln70His | |
| ENST00000651095.1:n.349G>T | ||
| ENST00000651196.1:c.210G>T | ENSP00000499096.1:p.Gln70His | |
| ENST00000651401.1:c.-1+404G>T | ENSP00000499115.1:n.-1+404G>T | |
| ENST00000651906.1:n.329G>T | ||
| ENST00000652237.1:n.329G>T | ||
| ENST00000252029.7:c.210G>T | ENSP00000252029.3:p.Gln70His | |
| ENST00000395678.7:c.210G>T | ENSP00000379036.3:p.Gln70His | |
| ENST00000395680.5:c.210G>T | ENSP00000379037.1:p.Gln70His | |
| ENST00000395681.5:c.210G>T | ENSP00000379038.1:p.Gln70His | |
| ENST00000425169.1:c.210G>T | ENSP00000395875.1:p.Gln70His | |
| ENST00000476284.1:n.335G>T | ||
| ENST00000487162.1:n.341G>T | ||
| ENST00000487577.5:n.497G>T | ||
| NM_001113755.2:c.210G>T | NP_001107227.1:p.Gln70His | |
| NM_001113756.2:c.210G>T | NP_001107228.1:p.Gln70His | |
| NM_001257988.1:c.210G>T , LRG_727t1:c.210G>T | NP_001244917.1:p.Gln70His | |
| NM_001257989.1:c.210G>T , LRG_727t2:c.210G>T | NP_001244918.1:p.Gln70His | |
| NM_001953.4:c.210G>T | NP_001944.1:p.Gln70His | |
| NM_001113755.3:c.210G>T | NP_001107227.1:p.Gln70His | |
| NM_001113756.3:c.210G>T | NP_001107228.1:p.Gln70His | |
| NM_001953.5:c.210G>T MANE Select | NP_001944.1:p.Gln70His |