Linked Data
ClinVar Variation Id:
180185
ClinVar RCV Id:
RCV000157037
dbSNP Id:
rs730880028
gnomAD v2:
2-220115778-G-A
gnomAD v4:
2-219251056-G-A
PubMed:
PMID:25374358
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219251056G>A , CM000664.2:g.219251056G>A | GRCh38 |
| NC_000002.11:g.220115778G>A , CM000664.1:g.220115778G>A | GRCh37 |
| NC_000002.10:g.219824022G>A | NCBI36 |
| NG_029913.1:g.7861C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248437.9:c.643C>T MANE Select | ENSP00000248437.4:p.Arg215Cys | |
| ENST00000248437.8:c.643C>T | ENSP00000248437.4:p.Arg215Cys | |
| ENST00000392088.6:c.598C>T | ENSP00000375938.2:p.Arg200Cys | |
| ENST00000398989.2:c.184C>T | ENSP00000396212.1:p.Arg62Cys | |
| ENST00000498660.1:n.463C>T | ||
| NM_001278552.1:c.598C>T | NP_001265481.1:p.Arg200Cys | |
| NM_006000.2:c.643C>T | NP_005991.1:p.Arg215Cys | |
| XM_005246832.1:c.598C>T | XP_005246889.1:p.Arg200Cys | |
| XM_017004824.1:c.184C>T | XP_016860313.1:p.Arg62Cys | |
| NM_006000.3:c.643C>T MANE Select | NP_005991.1:p.Arg215Cys | |
| NM_001278552.2:c.598C>T | NP_001265481.1:p.Arg200Cys |