Linked Data
ClinVar Variation Id:
30896
ClinVar RCV Id:
RCV000023882
dbSNP Id:
rs387907044
gnomAD v2:
15-90193041-G-A
gnomAD v4:
15-89649810-G-A
COSMIC:
COSM3706810
PubMed:
PMID:21552264
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89649810G>A , CM000677.2:g.89649810G>A | GRCh38 |
| NC_000015.9:g.90193041G>A , CM000677.1:g.90193041G>A | GRCh37 |
| NC_000015.8:g.87994045G>A | NCBI36 |
| NG_030338.1:g.10642C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696512.1:c.583C>T | ENSP00000512678.1:p.Arg195Ter | |
| ENST00000394412.8:c.460C>T MANE Select | ENSP00000377934.3:p.Arg154Ter | |
| ENST00000394412.7:c.460C>T | ENSP00000377934.3:p.Arg154Ter | |
| ENST00000445906.1:c.*119C>T | ENSP00000395906.1:n.*119C>T | |
| NM_198525.2:c.460C>T | NP_940927.2:p.Arg154Ter | |
| XM_005254902.2:c.460C>T | XP_005254959.1:p.Arg154Ter | |
| XM_011521531.1:c.583C>T | XP_011519833.1:p.Arg195Ter | |
| XM_011521532.1:c.583C>T | XP_011519834.1:p.Arg195Ter | |
| XM_011521533.1:c.583C>T | XP_011519835.1:p.Arg195Ter | |
| XM_011521534.1:c.583C>T | XP_011519836.1:p.Arg195Ter | |
| XM_011521535.1:c.583C>T | XP_011519837.1:p.Arg195Ter | |
| XM_011521536.1:c.583C>T | XP_011519838.1:p.Arg195Ter | |
| XM_011521537.1:c.583C>T | XP_011519839.1:p.Arg195Ter | |
| XM_011521531.2:c.583C>T | XP_011519833.1:p.Arg195Ter | |
| NM_198525.3:c.460C>T MANE Select | NP_940927.2:p.Arg154Ter |