Linked Data
ClinVar Variation Id:
135694
ClinVar RCV Id:
RCV000122768
RCV000485846
RCV000664308
RCV000574171
RCV001157044
RCV003315799
RCV003997374
RCV003325185
dbSNP Id:
rs587780593
gnomAD v2:
5-112173949-G-T
gnomAD v3:
5-112838252-G-T
gnomAD v4:
5-112838252-G-T
COSMIC:
COSM1432214
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838252G>T , CM000667.2:g.112838252G>T | GRCh38 |
| NC_000005.9:g.112173949G>T , CM000667.1:g.112173949G>T | GRCh37 |
| NC_000005.8:g.112201848G>T | NCBI36 |
| NG_008481.4:g.150732G>T , LRG_130:g.150732G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2323G>T | ENSP00000484935.2:n.2323G>T | |
| ENST00000504915.3:c.2712G>T | ENSP00000473355.2:p.Gln904His | |
| ENST00000505350.2:c.*2664G>T | ENSP00000481752.1:n.*2664G>T | |
| ENST00000507379.6:c.2604G>T | ENSP00000423224.2:p.Gln868His | |
| ENST00000509732.6:c.2658G>T | ENSP00000426541.2:p.Gln886His | |
| ENST00000512211.7:c.2658G>T | ENSP00000423828.3:p.Gln886His | |
| ENST00000257430.9:c.2658G>T MANE Select | ENSP00000257430.4:p.Gln886His | |
| ENST00000257430.8:c.2658G>T | ENSP00000257430.4:p.Gln886His | |
| ENST00000502371.2:c.1011G>T | ||
| ENST00000507379.5:c.2604G>T | ENSP00000423224.1:p.Gln868His | |
| ENST00000508376.6:c.2658G>T | ENSP00000427089.2:p.Gln886His | |
| ENST00000508624.5:c.*1980G>T | ENSP00000424265.1:n.*1980G>T | |
| ENST00000512211.6:c.2658G>T | ENSP00000423828.2:p.Gln886His | |
| ENST00000520401.1:c.230+9280G>T | ||
| NM_000038.5:c.2658G>T | NP_000029.2:p.Gln886His | |
| NM_001127510.2:c.2658G>T | NP_001120982.1:p.Gln886His | |
| NM_001127511.2:c.2604G>T | NP_001120983.2:p.Gln868His | |
| NM_001354895.1:c.2658G>T | NP_001341824.1:p.Gln886His | |
| NM_001354896.1:c.2712G>T | NP_001341825.1:p.Gln904His | |
| NM_001354897.1:c.2688G>T | NP_001341826.1:p.Gln896His | |
| NM_001354898.1:c.2583G>T | NP_001341827.1:p.Gln861His | |
| NM_001354899.1:c.2574G>T | NP_001341828.1:p.Gln858His | |
| NM_001354900.1:c.2535G>T | NP_001341829.1:p.Gln845His | |
| NM_001354901.1:c.2481G>T | NP_001341830.1:p.Gln827His | |
| NM_001354902.1:c.2385G>T | NP_001341831.1:p.Gln795His | |
| NM_001354903.1:c.2355G>T | NP_001341832.1:p.Gln785His | |
| NM_001354904.1:c.2280G>T | NP_001341833.1:p.Gln760His | |
| NM_001354905.1:c.2178G>T | NP_001341834.1:p.Gln726His | |
| NM_001354906.1:c.1809G>T | NP_001341835.1:p.Gln603His | |
| NM_000038.6:c.2658G>T MANE Select | NP_000029.2:p.Gln886His | |
| NM_001127510.3:c.2658G>T | NP_001120982.1:p.Gln886His | |
| NM_001127511.3:c.2604G>T | NP_001120983.2:p.Gln868His | |
| NM_001354895.2:c.2658G>T | NP_001341824.1:p.Gln886His | |
| NM_001354896.2:c.2712G>T | NP_001341825.1:p.Gln904His | |
| NM_001354897.2:c.2688G>T | NP_001341826.1:p.Gln896His | |
| NM_001354898.2:c.2583G>T | NP_001341827.1:p.Gln861His | |
| NM_001354899.2:c.2574G>T | NP_001341828.1:p.Gln858His | |
| NM_001354900.2:c.2535G>T | NP_001341829.1:p.Gln845His | |
| NM_001354901.2:c.2481G>T | NP_001341830.1:p.Gln827His | |
| NM_001354902.2:c.2385G>T | NP_001341831.1:p.Gln795His | |
| NM_001354903.2:c.2355G>T | NP_001341832.1:p.Gln785His | |
| NM_001354904.2:c.2280G>T | NP_001341833.1:p.Gln760His | |
| NM_001354905.2:c.2178G>T | NP_001341834.1:p.Gln726His | |
| NM_001354906.2:c.1809G>T | NP_001341835.1:p.Gln603His |