Linked Data
ClinVar Variation Id:
128130
ClinVar RCV Id:
RCV000116084
RCV000200135
RCV000212811
RCV000780574
RCV001354155
RCV000292657
RCV004542829
dbSNP Id:
rs377626805
ExAC:
16:23641096 G / A
gnomAD v2:
16-23641096-G-A
gnomAD v3:
16-23629775-G-A
gnomAD v4:
16-23629775-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23629775G>A , CM000678.2:g.23629775G>A | GRCh38 |
| NC_000016.9:g.23641096G>A , CM000678.1:g.23641096G>A | GRCh37 |
| NC_000016.8:g.23548597G>A | NCBI36 |
| NG_007406.1:g.16583C>T , LRG_308:g.16583C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.2385C>T | ENSP00000460666.3:p.Gly795= | |
| ENST00000565038.2:c.212-500C>T | ENSP00000459882.2:n.212-500C>T | |
| ENST00000566069.6:c.2379C>T | ENSP00000459237.2:p.Gly793= | |
| ENST00000697377.2:c.2385C>T | ENSP00000513286.2:p.Gly795= | |
| ENST00000697379.2:c.2385C>T | ENSP00000513287.2:p.Gly795= | |
| ENST00000561514.2:c.1494C>T | ENSP00000460666.2:p.Gly498= | |
| ENST00000697374.1:c.1494C>T | ENSP00000513284.1:p.Gly498= | |
| ENST00000697375.1:n.3726C>T | ||
| ENST00000697376.1:c.1494C>T | ENSP00000513285.1:p.Gly498= | |
| ENST00000697377.1:c.1494C>T | ENSP00000513286.1:p.Gly498= | |
| ENST00000697378.1:n.2899C>T | ||
| ENST00000697379.1:c.1494C>T | ENSP00000513287.1:p.Gly498= | |
| ENST00000697380.1:n.1307C>T | ||
| ENST00000697381.1:n.1074C>T | ||
| ENST00000697382.1:c.1494C>T | ENSP00000513288.1:p.Gly498= | |
| ENST00000697383.1:c.49-500C>T | ENSP00000513289.1:n.49-500C>T | |
| ENST00000697384.1:n.2533C>T | ||
| ENST00000261584.9:c.2379C>T MANE Select | ENSP00000261584.4:p.Gly793= | |
| ENST00000261584.8:c.2379C>T | ENSP00000261584.4:p.Gly793= | |
| ENST00000565038.1:c.87-500C>T | ||
| ENST00000568219.5:c.1494C>T | ENSP00000454703.2:p.Gly498= | |
| NM_024675.3:c.2379C>T , LRG_308t1:c.2379C>T | NP_078951.2:p.Gly793= | |
| XM_011545946.1:c.2385C>T | XP_011544248.1:p.Gly795= | |
| XM_011545947.1:c.2385C>T | XP_011544249.1:p.Gly795= | |
| XM_011545948.1:c.1494C>T | XP_011544250.1:p.Gly498= | |
| XR_950851.1:n.3175C>T | ||
| XM_011545946.2:c.2385C>T | XP_011544248.1:p.Gly795= | |
| XM_011545947.2:c.2385C>T | XP_011544249.1:p.Gly795= | |
| XM_011545948.2:c.1494C>T | XP_011544250.1:p.Gly498= | |
| XM_017023671.1:c.2385C>T | XP_016879160.1:p.Gly795= | |
| XM_017023672.2:c.2379C>T | XP_016879161.1:p.Gly793= | |
| XM_017023673.2:c.2379C>T | XP_016879162.1:p.Gly793= | |
| NM_024675.4:c.2379C>T MANE Select | NP_078951.2:p.Gly793= |