Linked Data
ClinVar Variation Id:
216014
ClinVar RCV Id:
RCV000236362
RCV000438475
RCV000492041
RCV000500904
RCV001000185
RCV002228900
RCV002288811
dbSNP Id:
rs121913333
COSMIC:
COSM18852
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838220C>T , CM000667.2:g.112838220C>T | GRCh38 |
| NC_000005.9:g.112173917C>T , CM000667.1:g.112173917C>T | GRCh37 |
| NC_000005.8:g.112201816C>T | NCBI36 |
| NG_008481.4:g.150700C>T , LRG_130:g.150700C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2291C>T | ENSP00000484935.2:n.2291C>T | |
| ENST00000504915.3:c.2680C>T | ENSP00000473355.2:p.Arg894Ter | |
| ENST00000505350.2:c.*2632C>T | ENSP00000481752.1:n.*2632C>T | |
| ENST00000507379.6:c.2572C>T | ENSP00000423224.2:p.Arg858Ter | |
| ENST00000509732.6:c.2626C>T | ENSP00000426541.2:p.Arg876Ter | |
| ENST00000512211.7:c.2626C>T | ENSP00000423828.3:p.Arg876Ter | |
| ENST00000257430.9:c.2626C>T MANE Select | ENSP00000257430.4:p.Arg876Ter | |
| ENST00000257430.8:c.2626C>T | ENSP00000257430.4:p.Arg876Ter | |
| ENST00000502371.2:c.979C>T | ||
| ENST00000507379.5:c.2572C>T | ENSP00000423224.1:p.Arg858Ter | |
| ENST00000508376.6:c.2626C>T | ENSP00000427089.2:p.Arg876Ter | |
| ENST00000508624.5:c.*1948C>T | ENSP00000424265.1:n.*1948C>T | |
| ENST00000512211.6:c.2626C>T | ENSP00000423828.2:p.Arg876Ter | |
| ENST00000520401.1:c.230+9248C>T | ||
| NM_000038.5:c.2626C>T | NP_000029.2:p.Arg876Ter | |
| NM_001127510.2:c.2626C>T | NP_001120982.1:p.Arg876Ter | |
| NM_001127511.2:c.2572C>T | NP_001120983.2:p.Arg858Ter | |
| NM_001354895.1:c.2626C>T | NP_001341824.1:p.Arg876Ter | |
| NM_001354896.1:c.2680C>T | NP_001341825.1:p.Arg894Ter | |
| NM_001354897.1:c.2656C>T | NP_001341826.1:p.Arg886Ter | |
| NM_001354898.1:c.2551C>T | NP_001341827.1:p.Arg851Ter | |
| NM_001354899.1:c.2542C>T | NP_001341828.1:p.Arg848Ter | |
| NM_001354900.1:c.2503C>T | NP_001341829.1:p.Arg835Ter | |
| NM_001354901.1:c.2449C>T | NP_001341830.1:p.Arg817Ter | |
| NM_001354902.1:c.2353C>T | NP_001341831.1:p.Arg785Ter | |
| NM_001354903.1:c.2323C>T | NP_001341832.1:p.Arg775Ter | |
| NM_001354904.1:c.2248C>T | NP_001341833.1:p.Arg750Ter | |
| NM_001354905.1:c.2146C>T | NP_001341834.1:p.Arg716Ter | |
| NM_001354906.1:c.1777C>T | NP_001341835.1:p.Arg593Ter | |
| NM_000038.6:c.2626C>T MANE Select | NP_000029.2:p.Arg876Ter | |
| NM_001127510.3:c.2626C>T | NP_001120982.1:p.Arg876Ter | |
| NM_001127511.3:c.2572C>T | NP_001120983.2:p.Arg858Ter | |
| NM_001354895.2:c.2626C>T | NP_001341824.1:p.Arg876Ter | |
| NM_001354896.2:c.2680C>T | NP_001341825.1:p.Arg894Ter | |
| NM_001354897.2:c.2656C>T | NP_001341826.1:p.Arg886Ter | |
| NM_001354898.2:c.2551C>T | NP_001341827.1:p.Arg851Ter | |
| NM_001354899.2:c.2542C>T | NP_001341828.1:p.Arg848Ter | |
| NM_001354900.2:c.2503C>T | NP_001341829.1:p.Arg835Ter | |
| NM_001354901.2:c.2449C>T | NP_001341830.1:p.Arg817Ter | |
| NM_001354902.2:c.2353C>T | NP_001341831.1:p.Arg785Ter | |
| NM_001354903.2:c.2323C>T | NP_001341832.1:p.Arg775Ter | |
| NM_001354904.2:c.2248C>T | NP_001341833.1:p.Arg750Ter | |
| NM_001354905.2:c.2146C>T | NP_001341834.1:p.Arg716Ter | |
| NM_001354906.2:c.1777C>T | NP_001341835.1:p.Arg593Ter |