Linked Data
ClinVar Variation Id:
1613157
ClinVar RCV Id:
RCV002183118
dbSNP Id:
rs1845849397
gnomAD v3:
11-1759550-G-A
gnomAD v4:
11-1759550-G-A
MyVariant Identifiers:
chr11:g.1780780G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1759550G>A , CM000673.2:g.1759550G>A | GRCh38 |
| NC_000011.9:g.1780780G>A , CM000673.1:g.1780780G>A | GRCh37 |
| NC_000011.8:g.1737356G>A | NCBI36 |
| NG_008655.1:g.9443C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236671.7:c.318C>T MANE Select | ENSP00000236671.2:p.Pro106= | |
| ENST00000367196.4:c.213C>T | ENSP00000356164.4:p.Pro71= | |
| ENST00000429746.2:c.213C>T | ENSP00000402586.2:p.Pro71= | |
| ENST00000433655.6:c.318C>T | ENSP00000404902.1:p.Pro106= | |
| ENST00000438213.6:c.318C>T | ENSP00000415036.2:p.Pro106= | |
| ENST00000636397.1:c.318C>T | ENSP00000489910.1:p.Pro106= | |
| ENST00000636571.1:c.297C>T | ENSP00000490770.1:p.Pro99= | |
| ENST00000636615.1:c.318C>T | ENSP00000490014.1:p.Pro106= | |
| ENST00000636843.1:c.312C>T | ENSP00000490897.1:p.Pro104= | |
| ENST00000637381.2:n.2746C>T | ||
| ENST00000637387.1:c.318C>T | ENSP00000490598.1:p.Pro106= | |
| ENST00000637815.2:c.318C>T | ENSP00000490344.1:p.Pro106= | |
| ENST00000637915.1:c.318C>T | ENSP00000490471.1:p.Pro106= | |
| ENST00000677300.1:n.713C>T | ||
| ENST00000678991.1:c.*179C>T | ENSP00000503019.1:n.*179C>T | |
| ENST00000236671.6:c.318C>T | ENSP00000236671.2:p.Pro106= | |
| ENST00000367196.3:c.213C>T | ENSP00000356164.3:p.Pro71= | |
| ENST00000433655.5:c.318C>T | ENSP00000404902.1:p.Pro106= | |
| ENST00000438213.5:c.273C>T | ENSP00000415036.1:p.Pro91= | |
| NM_001909.4:c.318C>T | NP_001900.1:p.Pro106= | |
| NM_001909.5:c.318C>T MANE Select | NP_001900.1:p.Pro106= |