Linked Data
ClinVar Variation Id:
2573820
ClinVar RCV Id:
RCV003318156
dbSNP Id:
rs769603145
COSMIC:
COSM735072
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112842803G>C , CM000667.2:g.112842803G>C | GRCh38 |
| NC_000005.9:g.112178500G>C , CM000667.1:g.112178500G>C | GRCh37 |
| NC_000005.8:g.112206399G>C | NCBI36 |
| NG_008481.4:g.155283G>C , LRG_130:g.155283G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7263G>C | ENSP00000473355.2:p.Gln2421His | |
| ENST00000505350.2:c.*7215G>C | ENSP00000481752.1:n.*7215G>C | |
| ENST00000507379.6:c.7155G>C | ENSP00000423224.2:p.Gln2385His | |
| ENST00000509732.6:c.7209G>C | ENSP00000426541.2:p.Gln2403His | |
| ENST00000512211.7:c.7209G>C | ENSP00000423828.3:p.Gln2403His | |
| ENST00000257430.9:c.7209G>C MANE Select | ENSP00000257430.4:p.Gln2403His | |
| ENST00000257430.8:c.7209G>C | ENSP00000257430.4:p.Gln2403His | |
| ENST00000508376.6:c.7209G>C | ENSP00000427089.2:p.Gln2403His | |
| ENST00000520401.1:c.230+13831G>C | ||
| NM_000038.5:c.7209G>C | NP_000029.2:p.Gln2403His | |
| NM_001127510.2:c.7209G>C | NP_001120982.1:p.Gln2403His | |
| NM_001127511.2:c.7155G>C | NP_001120983.2:p.Gln2385His | |
| NM_001354895.1:c.7209G>C | NP_001341824.1:p.Gln2403His | |
| NM_001354896.1:c.7263G>C | NP_001341825.1:p.Gln2421His | |
| NM_001354897.1:c.7239G>C | NP_001341826.1:p.Gln2413His | |
| NM_001354898.1:c.7134G>C | NP_001341827.1:p.Gln2378His | |
| NM_001354899.1:c.7125G>C | NP_001341828.1:p.Gln2375His | |
| NM_001354900.1:c.7086G>C | NP_001341829.1:p.Gln2362His | |
| NM_001354901.1:c.7032G>C | NP_001341830.1:p.Gln2344His | |
| NM_001354902.1:c.6936G>C | NP_001341831.1:p.Gln2312His | |
| NM_001354903.1:c.6906G>C | NP_001341832.1:p.Gln2302His | |
| NM_001354904.1:c.6831G>C | NP_001341833.1:p.Gln2277His | |
| NM_001354905.1:c.6729G>C | NP_001341834.1:p.Gln2243His | |
| NM_001354906.1:c.6360G>C | NP_001341835.1:p.Gln2120His | |
| NM_000038.6:c.7209G>C MANE Select | NP_000029.2:p.Gln2403His | |
| NM_001127510.3:c.7209G>C | NP_001120982.1:p.Gln2403His | |
| NM_001127511.3:c.7155G>C | NP_001120983.2:p.Gln2385His | |
| NM_001354895.2:c.7209G>C | NP_001341824.1:p.Gln2403His | |
| NM_001354896.2:c.7263G>C | NP_001341825.1:p.Gln2421His | |
| NM_001354897.2:c.7239G>C | NP_001341826.1:p.Gln2413His | |
| NM_001354898.2:c.7134G>C | NP_001341827.1:p.Gln2378His | |
| NM_001354899.2:c.7125G>C | NP_001341828.1:p.Gln2375His | |
| NM_001354900.2:c.7086G>C | NP_001341829.1:p.Gln2362His | |
| NM_001354901.2:c.7032G>C | NP_001341830.1:p.Gln2344His | |
| NM_001354902.2:c.6936G>C | NP_001341831.1:p.Gln2312His | |
| NM_001354903.2:c.6906G>C | NP_001341832.1:p.Gln2302His | |
| NM_001354904.2:c.6831G>C | NP_001341833.1:p.Gln2277His | |
| NM_001354905.2:c.6729G>C | NP_001341834.1:p.Gln2243His | |
| NM_001354906.2:c.6360G>C | NP_001341835.1:p.Gln2120His |