Linked Data
ClinVar Variation Id:
13306
ClinVar RCV Id:
RCV002468927
dbSNP Id:
rs121918480
PubMed:
PMID:2719946
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46739341G>T , CM000673.2:g.46739341G>T | GRCh38 |
| NC_000011.9:g.46760891G>T , CM000673.1:g.46760891G>T | GRCh37 |
| NC_000011.8:g.46717467G>T | NCBI36 |
| NG_008953.1:g.25149G>T , LRG_551:g.25149G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311907.10:c.1802G>T MANE Select | ENSP00000308541.5:p.Gly601Val | |
| ENST00000311907.9:c.1802G>T | ENSP00000308541.5:p.Gly601Val | |
| ENST00000530231.5:c.1685G>T | ENSP00000433907.1:p.Gly562Val | |
| NM_000506.3:c.1802G>T | NP_000497.1:p.Gly601Val | |
| NM_000506.4:c.1802G>T , LRG_551t1:c.1802G>T | NP_000497.1:p.Gly601Val | |
| NM_001311257.1:c.1754G>T | NP_001298186.1:p.Gly585Val | |
| XR_428840.2:n.1664G>T | ||
| XR_428840.4:n.1655G>T | ||
| NM_000506.5:c.1802G>T MANE Select | NP_000497.1:p.Gly601Val | |
| NM_001311257.2:c.1754G>T | NP_001298186.1:p.Gly585Val |