Linked Data
ClinVar Variation Id:
2733560
ClinVar RCV Id:
RCV003518709
dbSNP Id:
rs1329792379
gnomAD v2:
13-48563103-G-A
gnomAD v3:
13-47988968-G-A
gnomAD v4:
13-47988968-G-A
COSMIC:
COSM1477247
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.47988968G>A , CM000675.2:g.47988968G>A | GRCh38 |
| NC_000013.10:g.48563103G>A , CM000675.1:g.48563103G>A | GRCh37 |
| NC_000013.9:g.47461104G>A | NCBI36 |
| NG_008241.1:g.17360C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642944.1:c.111C>T | ENSP00000495674.1:p.Val37= | |
| ENST00000643023.1:c.285C>T | ENSP00000495664.1:p.Val95= | |
| ENST00000643584.1:c.285C>T | ENSP00000494987.1:p.Val95= | |
| ENST00000644338.1:c.285C>T | ENSP00000494723.1:p.Val95= | |
| ENST00000646602.1:c.285C>T | ENSP00000495250.1:p.Val95= | |
| ENST00000646804.1:c.111C>T | ENSP00000493977.1:p.Val37= | |
| ENST00000646932.1:c.285C>T MANE Select | ENSP00000494360.1:p.Val95= | |
| ENST00000647361.1:c.*78C>T | ENSP00000494607.1:n.*78C>T | |
| ENST00000378654.8:c.285C>T | ENSP00000367923.3:p.Val95= | |
| ENST00000433022.1:c.90+12212C>T | ENSP00000415091.1:n.90+12212C>T | |
| ENST00000434484.5:c.75C>T | ENSP00000392771.1:p.Val25= | |
| ENST00000470760.2:c.285C>T | ENSP00000488974.1:p.Val95= | |
| ENST00000497202.6:c.379C>T | ENSP00000489175.1:p.Arg127Cys | |
| NM_003850.2:c.285C>T | NP_003841.1:p.Val95= | |
| XM_011535292.1:c.48C>T | XP_011533594.1:p.Val16= | |
| XM_011535293.1:c.-118C>T | XP_011533595.1:n.-118C>T | |
| XR_941688.1:n.329C>T | ||
| NM_003850.3:c.285C>T MANE Select | NP_003841.1:p.Val95= |