Linked Data
ClinVar Variation Id:
433316
ClinVar RCV Id:
RCV000499087
dbSNP Id:
rs60791294
PubMed:
PMID:11536079
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16163086C>G , CM000678.2:g.16163086C>G | GRCh38 |
| NC_000016.9:g.16256943C>G , CM000678.1:g.16256943C>G | GRCh37 |
| NC_000016.8:g.16164444C>G | NCBI36 |
| NG_007558.2:g.65386G>C | |
| NG_007558.3:g.65532G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.3413G>C | ENSP00000483331.2:p.Arg1138Pro | |
| ENST00000205557.12:c.3413G>C MANE Select | ENSP00000205557.7:p.Arg1138Pro | |
| ENST00000640696.1:c.321-1522G>C | ENSP00000492197.1:n.321-1522G>C | |
| ENST00000205557.11:c.3413G>C | ENSP00000205557.7:p.Arg1138Pro | |
| ENST00000456970.6:c.3132-1522G>C | ENSP00000405002.2:n.3132-1522G>C | |
| ENST00000622290.4:c.*622G>C | ENSP00000483331.1:n.*622G>C | |
| NM_001171.5:c.3413G>C | NP_001162.4:p.Arg1138Pro | |
| XM_011522479.1:c.3380G>C | XP_011520781.1:p.Arg1127Pro | |
| XM_011522480.1:c.3071G>C | XP_011520782.1:p.Arg1024Pro | |
| XM_011522481.1:c.3071G>C | XP_011520783.1:p.Arg1024Pro | |
| XR_932836.1:n.3648G>C | ||
| XR_932837.1:n.3543-1522G>C | ||
| XR_932838.1:n.3543-1522G>C | ||
| XR_933133.1:n.407+243C>G | ||
| XR_933134.1:n.754+243C>G | ||
| NM_001351800.1:c.3071G>C | NP_001338729.1:p.Arg1024Pro | |
| NR_147784.1:n.3169-1522G>C | ||
| XM_011522479.2:c.3380G>C | XP_011520781.1:p.Arg1127Pro | |
| XM_011522481.3:c.3071G>C | XP_011520783.1:p.Arg1024Pro | |
| XM_017023212.1:c.3245G>C | XP_016878701.1:p.Arg1082Pro | |
| XM_017023214.1:c.3307-1522G>C | XP_016878703.1:n.3307-1522G>C | |
| XM_024450261.1:c.3449G>C | XP_024306029.1:p.Arg1150Pro | |
| XR_932836.2:n.3594G>C | ||
| XR_932837.3:n.3488-1522G>C | ||
| XR_932838.3:n.3488-1522G>C | ||
| NM_001171.6:c.3413G>C MANE Select | NP_001162.5:p.Arg1138Pro |