Linked Data
ClinVar Variation Id:
956732
ClinVar RCV Id:
RCV001229593
dbSNP Id:
rs189313574
ExAC:
5:158747500 C / T
gnomAD v2:
5-158747500-C-T
gnomAD v3:
5-159320492-C-T
gnomAD v4:
5-159320492-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320492C>T , CM000667.2:g.159320492C>T | GRCh38 |
| NC_000005.9:g.158747500C>T , CM000667.1:g.158747500C>T | GRCh37 |
| NC_000005.8:g.158680078C>T | NCBI36 |
| NG_009618.1:g.14982G>A , LRG_71:g.14982G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-120G>A | ENSP00000512849.1:n.-120G>A | |
| ENST00000696751.1:c.*6G>A | ENSP00000512850.1:n.*6G>A | |
| ENST00000231228.3:c.511G>A MANE Select | ENSP00000231228.2:p.Gly171Arg | |
| ENST00000231228.2:c.511G>A | ENSP00000231228.2:p.Gly171Arg | |
| NM_002187.2:c.511G>A , LRG_71t1:c.511G>A | NP_002178.2:p.Gly171Arg | |
| XR_001742945.1:n.43C>T | ||
| NM_002187.3:c.511G>A MANE Select | NP_002178.2:p.Gly171Arg |