Linked Data
ClinVar Variation Id:
291348
ClinVar RCV Id:
RCV000400990
dbSNP Id:
rs886044922
gnomAD v3:
1-99916612-T-C
gnomAD v4:
1-99916612-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.99916612T>C , CM000663.2:g.99916612T>C | GRCh38 |
| NC_000001.10:g.100382168T>C , CM000663.1:g.100382168T>C | GRCh37 |
| NC_000001.9:g.100154756T>C | NCBI36 |
| NG_012865.1:g.71529T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361915.8:c.4362T>C MANE Select | ENSP00000355106.3:p.Pro1454= | |
| ENST00000637337.1:n.4573T>C | ||
| ENST00000294724.8:c.4362T>C | ENSP00000294724.4:p.Pro1454= | |
| ENST00000361302.7:c.4314T>C | ENSP00000354971.3:p.Pro1438= | |
| ENST00000361522.4:c.4311T>C | ENSP00000354635.4:p.Pro1437= | |
| ENST00000361915.7:c.4362T>C | ENSP00000355106.3:p.Pro1454= | |
| ENST00000370161.6:c.4314T>C | ENSP00000359180.2:p.Pro1438= | |
| ENST00000370163.7:c.4362T>C | ENSP00000359182.3:p.Pro1454= | |
| ENST00000370165.7:c.4362T>C | ENSP00000359184.3:p.Pro1454= | |
| NM_000028.2:c.4362T>C | NP_000019.2:p.Pro1454= | |
| NM_000642.2:c.4362T>C | NP_000633.2:p.Pro1454= | |
| NM_000643.2:c.4362T>C | NP_000634.2:p.Pro1454= | |
| NM_000644.2:c.4362T>C | NP_000635.2:p.Pro1454= | |
| NM_000645.2:c.4311T>C | NP_000636.2:p.Pro1437= | |
| NM_000646.2:c.4314T>C | NP_000637.2:p.Pro1438= | |
| XM_005270557.1:c.4362T>C | XP_005270614.1:p.Pro1454= | |
| XR_947626.1:n.1318-3395A>G | ||
| XR_947627.1:n.1207-3395A>G | ||
| XR_947628.1:n.1312-3395A>G | ||
| XR_947630.1:n.1250-3395A>G | ||
| XR_947632.1:n.1136-3395A>G | ||
| XR_947633.1:n.1247-3395A>G | ||
| XR_947634.1:n.661-3395A>G | ||
| XR_947635.1:n.729-3395A>G | ||
| XM_005270557.2:c.4362T>C | XP_005270614.1:p.Pro1454= | |
| XM_017000501.2:c.2622T>C | XP_016855990.1:p.Pro874= | |
| NM_000642.3:c.4362T>C MANE Select | NP_000633.2:p.Pro1454= |