Linked Data
ClinVar Variation Id:
1445521
ClinVar RCV Id:
RCV001958282
dbSNP Id:
rs560833188
ExAC:
22:23915669 C / T
gnomAD v2:
22-23915669-C-T
gnomAD v3:
22-23573482-C-T
gnomAD v4:
22-23573482-C-T
PubMed:
PMID:27525107
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573482C>T , CM000684.2:g.23573482C>T | GRCh38 |
| NC_000022.10:g.23915669C>T , CM000684.1:g.23915669C>T | GRCh37 |
| NC_000022.9:g.22245669C>T | NCBI36 |
| NG_009791.1:g.11827G>A , LRG_69:g.11827G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330377.3:c.426G>A MANE Select | ENSP00000329312.2:p.Pro142= | |
| ENST00000249053.3:c.*55G>A | ENSP00000249053.3:n.*55G>A | |
| ENST00000330377.2:c.426G>A | ENSP00000329312.2:p.Pro142= | |
| ENST00000438703.1:c.429G>A | ENSP00000403391.1:p.Pro143= | |
| NM_020070.3:c.426G>A | NP_064455.1:p.Pro142= | |
| NM_152855.2:c.*55G>A | NP_690594.1:n.*55G>A | |
| XM_011530169.1:c.429G>A | XP_011528471.1:p.Pro143= | |
| XM_011530169.2:c.429G>A | XP_011528471.1:p.Pro143= | |
| NM_020070.4:c.426G>A MANE Select | NP_064455.1:p.Pro142= | |
| NM_001369906.1:c.429G>A | NP_001356835.1:p.Pro143= | |
| NM_152855.3:c.*55G>A | NP_690594.1:n.*55G>A |