Linked Data
ClinVar Variation Id:
97466
dbSNP Id:
rs104895135
ExAC:
16:3293660 G / C
gnomAD v2:
16-3293660-G-C
gnomAD v3:
16-3243660-G-C
gnomAD v4:
16-3243660-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3243660G>C , CM000678.2:g.3243660G>C | GRCh38 |
| NC_000016.9:g.3293660G>C , CM000678.1:g.3293660G>C | GRCh37 |
| NC_000016.8:g.3233661G>C | NCBI36 |
| NG_007871.1:g.17968C>G , LRG_190:g.17968C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697124.1:n.948C>G | ||
| ENST00000219596.6:c.1827C>G MANE Select | ENSP00000219596.1:p.Pro609= | |
| ENST00000219596.5:c.1827C>G | ENSP00000219596.1:p.Pro609= | |
| ENST00000339854.8:c.1287C>G | ENSP00000339639.4:p.Pro429= | |
| ENST00000536379.5:c.1194C>G | ENSP00000445079.1:p.Pro398= | |
| ENST00000536980.5:c.*103C>G | ENSP00000444178.1:n.*103C>G | |
| ENST00000537682.5:c.*103C>G | ENSP00000438611.1:n.*103C>G | |
| ENST00000538326.5:c.*452C>G | ENSP00000437486.1:n.*452C>G | |
| ENST00000539145.5:c.748C>G | ENSP00000444471.1:n.748C>G | |
| ENST00000541159.5:c.1369C>G | ENSP00000438711.1:n.1369C>G | |
| ENST00000542898.5:c.*103C>G | ENSP00000444615.1:n.*103C>G | |
| ENST00000570511.5:c.1232C>G | ENSP00000458312.1:n.1232C>G | |
| ENST00000572244.5:c.517C>G | ENSP00000461186.1:n.517C>G | |
| ENST00000574583.5:c.599C>G | ENSP00000460269.1:n.599C>G | |
| ENST00000576315.5:c.632C>G | ENSP00000460551.1:n.632C>G | |
| ENST00000621655.1:c.1364C>G | ENSP00000481436.1:n.1364C>G | |
| NM_000243.2:c.1827C>G , LRG_190t1:c.1827C>G | NP_000234.1:p.Pro609= | |
| NM_001198536.1:c.*31C>G | NP_001185465.1:n.*31C>G | |
| XM_017023236.2:c.1824C>G | XP_016878725.1:p.Pro608= | |
| XR_001751903.1:n.2134C>G | ||
| NM_000243.3:c.1827C>G MANE Select | NP_000234.1:p.Pro609= | |
| NM_001198536.2:c.*31C>G | NP_001185465.2:n.*31C>G |