Linked Data
ClinVar Variation Id:
12967
ClinVar RCV Id:
RCV000013833
RCV000013834
RCV000119625
RCV000806352
RCV001787706
RCV001787708
RCV001787710
RCV001787711
RCV001787402
RCV001787707
RCV001787709
RCV004017239
dbSNP Id:
rs118192161
gnomAD v4:
19-38444211-C-T
COSMIC:
COSM107248
ERepo:
CA018598/MONDO:0007783/012
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38444211C>T , CM000681.2:g.38444211C>T | GRCh38 |
| NC_000019.9:g.38934851C>T , CM000681.1:g.38934851C>T | GRCh37 |
| NC_000019.8:g.43626691C>T | NCBI36 |
| NG_008866.1:g.15512C>T , LRG_766:g.15512C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.487C>T | ENSP00000471601.2:p.Arg163Cys | |
| ENST00000359596.8:c.487C>T MANE Select | ENSP00000352608.2:p.Arg163Cys | |
| ENST00000355481.8:c.487C>T | ENSP00000347667.3:p.Arg163Cys | |
| ENST00000359596.7:c.487C>T | ENSP00000352608.2:p.Arg163Cys | |
| ENST00000360985.7:c.487C>T | ENSP00000354254.4:p.Arg163Cys | |
| NM_000540.2:c.487C>T , LRG_766t1:c.487C>T | NP_000531.2:p.Arg163Cys | |
| NM_001042723.1:c.487C>T | NP_001036188.1:p.Arg163Cys | |
| XM_006723317.1:c.487C>T | XP_006723380.1:p.Arg163Cys | |
| XM_006723319.1:c.487C>T | XP_006723382.1:p.Arg163Cys | |
| XM_011527204.1:c.487C>T | XP_011525506.1:p.Arg163Cys | |
| XM_011527205.1:c.487C>T | XP_011525507.1:p.Arg163Cys | |
| XM_006723317.2:c.487C>T | XP_006723380.1:p.Arg163Cys | |
| XM_006723319.2:c.487C>T | XP_006723382.1:p.Arg163Cys | |
| XM_011527205.2:c.487C>T | XP_011525507.1:p.Arg163Cys | |
| XR_001753735.1:n.570C>T | ||
| NM_000540.3:c.487C>T MANE Select | NP_000531.2:p.Arg163Cys | |
| NM_001042723.2:c.487C>T | NP_001036188.1:p.Arg163Cys |