Linked Data
ClinVar Variation Id:
425949
ClinVar RCV Id:
RCV000488860
dbSNP Id:
rs1085307357
PubMed:
PMID:26387786
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202552758C>T , CM000664.2:g.202552758C>T | GRCh38 |
| NC_000002.11:g.203417481C>T , CM000664.1:g.203417481C>T | GRCh37 |
| NC_000002.10:g.203125726C>T | NCBI36 |
| NG_009363.1:g.181432C>T , LRG_712:g.181432C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374580.10:c.1456C>T MANE Select | ENSP00000363708.4:p.Gln486Ter | |
| ENST00000638587.1:c.1387C>T | ENSP00000491062.1:p.Gln463Ter | |
| ENST00000374574.2:c.1456C>T | ENSP00000363702.2:p.Gln486Ter | |
| ENST00000374580.8:c.1456C>T | ENSP00000363708.4:p.Gln486Ter | |
| NM_001204.6:c.1456C>T , LRG_712t1:c.1456C>T | NP_001195.2:p.Gln486Ter | |
| XM_011511687.1:c.1456C>T | XP_011509989.1:p.Gln486Ter | |
| XM_011511688.1:c.1456C>T | XP_011509990.1:p.Gln486Ter | |
| NM_001204.7:c.1456C>T MANE Select | NP_001195.2:p.Gln486Ter |