Linked Data
ClinVar Variation Id:
1130795
ClinVar RCV Id:
RCV001464428
dbSNP Id:
rs761547868
ExAC:
19:4816326 C / T
gnomAD v2:
19-4816326-C-T
gnomAD v3:
19-4816314-C-T
gnomAD v4:
19-4816314-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816314C>T , CM000681.2:g.4816314C>T | GRCh38 |
| NC_000019.9:g.4816326C>T , CM000681.1:g.4816326C>T | GRCh37 |
| NC_000019.8:g.4767326C>T | NCBI36 |
| NG_031998.1:g.20429G>A , LRG_358:g.20429G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.2064G>A MANE Select | ENSP00000248244.4:p.Gln688= | |
| ENST00000248244.5:c.2064G>A | ENSP00000248244.4:p.Gln688= | |
| ENST00000621756.1:c.1566G>A | ENSP00000479467.1:p.Gln522= | |
| NM_182919.3:c.2064G>A , LRG_358t1:c.2064G>A | NP_891549.1:p.Gln688= | |
| NM_001385678.1:c.2022G>A | NP_001372607.1:p.Gln674= | |
| NM_001385679.1:c.1929G>A | NP_001372608.1:p.Gln643= | |
| NM_001385680.1:c.1422G>A | NP_001372609.1:p.Gln474= | |
| NM_182919.4:c.2064G>A MANE Select | NP_891549.1:p.Gln688= |