Linked Data
ClinVar Variation Id:
2761799
ClinVar RCV Id:
RCV003507728
dbSNP Id:
rs772944750
ExAC:
22:19751822 C / A
gnomAD v2:
22-19751822-C-A
gnomAD v3:
22-19764299-C-A
gnomAD v4:
22-19764299-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19764299C>A , CM000684.2:g.19764299C>A | GRCh38 |
| NC_000022.10:g.19751822C>A , CM000684.1:g.19751822C>A | GRCh37 |
| NC_000022.9:g.18131822C>A | NCBI36 |
| NG_009229.1:g.12597C>A , LRG_226:g.12597C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700274.1:c.210C>A | ENSP00000514909.1:p.Thr70= | |
| ENST00000649276.2:c.684C>A MANE Select | ENSP00000497003.1:p.Thr228= | |
| ENST00000680333.1:c.657C>A | ENSP00000505472.1:p.Thr219= | |
| ENST00000329705.11:c.657C>A | ENSP00000331176.7:p.Thr219= | |
| ENST00000332710.8:c.657C>A | ENSP00000331791.4:p.Thr219= | |
| ENST00000359500.7:c.657C>A | ENSP00000352483.3:p.Thr219= | |
| ENST00000621939.1:c.657C>A | ENSP00000477982.1:p.Thr219= | |
| NM_005992.1:c.657C>A | NP_005983.1:p.Thr219= | |
| NM_080646.1:c.657C>A | NP_542377.1:p.Thr219= | |
| NM_080647.1:c.657C>A , LRG_226t1:c.657C>A | NP_542378.1:p.Thr219= | |
| XM_006724312.1:c.657C>A | XP_006724375.1:p.Thr219= | |
| XM_011530351.1:c.684C>A | XP_011528653.1:p.Thr228= | |
| XM_006724312.2:c.657C>A | XP_006724375.1:p.Thr219= | |
| XM_017028925.1:c.807C>A | XP_016884414.1:p.Thr269= | |
| XM_017028926.1:c.657C>A | XP_016884415.1:p.Thr219= | |
| XM_017028928.1:c.807C>A | XP_016884417.1:p.Thr269= | |
| NM_001379200.1:c.684C>A MANE Select | NP_001366129.1:p.Thr228= | |
| NM_080646.2:c.657C>A | NP_542377.1:p.Thr219= |