Linked Data
ClinVar Variation Id:
1256271
ClinVar RCV Id:
RCV001663613
dbSNP Id:
rs143340609
ExAC:
9:71679936 T / C
gnomAD v2:
9-71679936-T-C
gnomAD v3:
9-69065020-T-C
gnomAD v4:
9-69065020-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.69065020T>C , CM000671.2:g.69065020T>C | GRCh38 |
| NC_000009.11:g.71679936T>C , CM000671.1:g.71679936T>C | GRCh37 |
| NC_000009.10:g.70869756T>C | NCBI36 |
| NG_008845.2:g.34458T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000377270.8:c.242T>C | ENSP00000366482.4:p.Leu81Pro | |
| ENST00000484259.3:c.467T>C MANE Select | ENSP00000419243.2:p.Leu156Pro | |
| ENST00000642330.1:c.384+11760T>C | ENSP00000493770.1:n.384+11760T>C | |
| ENST00000642889.1:c.165+29073T>C | ENSP00000493780.1:n.165+29073T>C | |
| ENST00000643352.1:c.467T>C | ENSP00000496488.1:p.Leu156Pro | |
| ENST00000643765.1:c.465T>C | ||
| ENST00000644653.1:c.*70T>C | ENSP00000495217.1:n.*70T>C | |
| ENST00000644977.1:c.*192T>C | ENSP00000495651.1:n.*192T>C | |
| ENST00000645088.1:c.*70T>C | ENSP00000495447.1:n.*70T>C | |
| ENST00000646862.1:c.384+11760T>C | ENSP00000494599.1:n.384+11760T>C | |
| ENST00000377270.7:c.467T>C | ENSP00000366482.3:p.Leu156Pro | |
| ENST00000396364.7:c.467T>C | ENSP00000379650.3:p.Leu156Pro | |
| ENST00000396366.6:c.467T>C | ENSP00000379652.2:p.Leu156Pro | |
| ENST00000484259.1:c.159T>C | ||
| ENST00000498653.5:c.242T>C | ENSP00000418015.1:p.Leu81Pro | |
| NM_000144.4:c.467T>C | NP_000135.2:p.Leu156Pro | |
| NM_001161706.1:c.467T>C | NP_001155178.1:p.Leu156Pro | |
| NM_181425.2:c.467T>C | NP_852090.1:p.Leu156Pro | |
| NM_000144.5:c.467T>C MANE Select | NP_000135.2:p.Leu156Pro | |
| NM_181425.3:c.467T>C | NP_852090.1:p.Leu156Pro |