Linked Data
ClinVar Variation Id:
97484
ClinVar RCV Id:
RCV000083736
dbSNP Id:
rs104895098
ExAC:
16:3293423 G / C
gnomAD v2:
16-3293423-G-C
gnomAD v4:
16-3243423-G-C
PubMed:
PMID:20301405
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3243423G>C , CM000678.2:g.3243423G>C | GRCh38 |
| NC_000016.9:g.3293423G>C , CM000678.1:g.3293423G>C | GRCh37 |
| NC_000016.8:g.3233424G>C | NCBI36 |
| NG_007871.1:g.18205C>G , LRG_190:g.18205C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697124.1:n.1185C>G | ||
| ENST00000219596.6:c.2064C>G MANE Select | ENSP00000219596.1:p.Tyr688Ter | |
| ENST00000219596.5:c.2064C>G | ENSP00000219596.1:p.Tyr688Ter | |
| ENST00000339854.8:c.1524C>G | ENSP00000339639.4:p.Tyr508Ter | |
| ENST00000536379.5:c.1431C>G | ENSP00000445079.1:p.Tyr477Ter | |
| ENST00000536980.5:c.*340C>G | ENSP00000444178.1:n.*340C>G | |
| ENST00000537682.5:c.*340C>G | ENSP00000438611.1:n.*340C>G | |
| ENST00000538326.5:c.*689C>G | ENSP00000437486.1:n.*689C>G | |
| ENST00000539145.5:c.985C>G | ENSP00000444471.1:n.985C>G | |
| ENST00000541159.5:c.1606C>G | ENSP00000438711.1:n.1606C>G | |
| ENST00000542898.5:c.*340C>G | ENSP00000444615.1:n.*340C>G | |
| ENST00000570511.5:c.1469C>G | ENSP00000458312.1:n.1469C>G | |
| ENST00000572244.5:c.754C>G | ENSP00000461186.1:n.754C>G | |
| ENST00000574583.5:c.836C>G | ENSP00000460269.1:n.836C>G | |
| ENST00000576315.5:c.869C>G | ENSP00000460551.1:n.869C>G | |
| ENST00000621655.1:c.1601C>G | ENSP00000481436.1:n.1601C>G | |
| NM_000243.2:c.2064C>G , LRG_190t1:c.2064C>G | NP_000234.1:p.Tyr688Ter | |
| NM_001198536.1:c.*268C>G | NP_001185465.1:n.*268C>G | |
| XM_017023236.2:c.2061C>G | XP_016878725.1:p.Tyr687Ter | |
| NM_000243.3:c.2064C>G MANE Select | NP_000234.1:p.Tyr688Ter | |
| NM_001198536.2:c.*268C>G | NP_001185465.2:n.*268C>G |