Linked Data
ClinVar Variation Id:
1460003
ClinVar RCV Id:
RCV001951371
dbSNP Id:
rs2151429138
PubMed:
PMID:23913538
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31229178A>T , CM000679.2:g.31229178A>T | GRCh38 |
| NC_000017.10:g.29556196A>T , CM000679.1:g.29556196A>T | GRCh37 |
| NC_000017.9:g.26580322A>T | NCBI36 |
| NG_009018.1:g.139202A>T , LRG_214:g.139202A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.2608A>T | ENSP00000512431.1:p.Arg870Ter | |
| ENST00000691014.1:c.2593A>T | ENSP00000510595.1:p.Arg865Ter | |
| ENST00000358273.9:c.2563A>T MANE Select | ENSP00000351015.4:p.Arg855Ter | |
| ENST00000356175.7:c.2563A>T | ENSP00000348498.3:p.Arg855Ter | |
| ENST00000358273.8:c.2563A>T | ENSP00000351015.4:p.Arg855Ter | |
| ENST00000456735.6:c.1561A>T | ENSP00000389907.2:p.Arg521Ter | |
| ENST00000493220.5:n.730A>T | ||
| ENST00000495910.6:c.2338A>T | ||
| ENST00000579081.5:c.2665A>T | ENSP00000462408.1:p.Arg889Ter | |
| NM_000267.3:c.2563A>T , LRG_214t1:c.2563A>T | NP_000258.1:p.Arg855Ter | |
| NM_001042492.2:c.2563A>T , LRG_214t2:c.2563A>T | NP_001035957.1:p.Arg855Ter | |
| XM_005257983.1:c.2563A>T | XP_005258040.1:p.Arg855Ter | |
| XM_005257984.1:c.2563A>T | XP_005258041.1:p.Arg855Ter | |
| XM_006721922.1:c.2593A>T | XP_006721985.1:p.Arg865Ter | |
| XM_006721923.2:c.2554A>T | XP_006721986.1:p.Arg852Ter | |
| XM_006721924.1:c.2593A>T | XP_006721987.1:p.Arg865Ter | |
| XM_006721925.1:c.2593A>T | XP_006721988.1:p.Arg865Ter | |
| XM_006721926.2:c.2593A>T | XP_006721989.1:p.Arg865Ter | |
| XM_006721927.1:c.2593A>T | XP_006721990.1:p.Arg865Ter | |
| XM_006721928.2:c.2593A>T | XP_006721991.1:p.Arg865Ter | |
| XM_011524852.1:c.2590A>T | XP_011523154.1:p.Arg864Ter | |
| XM_011524853.1:c.2554A>T | XP_011523155.1:p.Arg852Ter | |
| XM_011524854.1:c.2554A>T | XP_011523156.1:p.Arg852Ter | |
| XM_011524855.1:c.2554A>T | XP_011523157.1:p.Arg852Ter | |
| XM_011524856.1:c.2554A>T | XP_011523158.1:p.Arg852Ter | |
| XM_011524857.1:c.2593A>T | XP_011523159.1:p.Arg865Ter | |
| NM_001042492.3:c.2563A>T MANE Select | NP_001035957.1:p.Arg855Ter |