Linked Data
ClinVar Variation Id:
137623
ClinVar RCV Id:
RCV000125472
dbSNP Id:
rs587777447
PubMed:
PMID:24686847
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162288221T>C , CM000664.2:g.162288221T>C | GRCh38 |
| NC_000002.11:g.163144731T>C , CM000664.1:g.163144731T>C | GRCh37 |
| NC_000002.10:g.162852977T>C | NCBI36 |
| NG_011495.1:g.35309A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697291.1:c.*606A>G | ENSP00000513228.1:n.*606A>G | |
| ENST00000648433.1:c.1009A>G | ENSP00000496816.1:p.Arg337Gly | |
| ENST00000649554.1:n.619A>G | ||
| ENST00000649979.2:c.1009A>G MANE Select | ENSP00000497271.1:p.Arg337Gly | |
| ENST00000679938.1:c.697A>G | ENSP00000505518.1:p.Arg233Gly | |
| ENST00000263642.2:c.1009A>G | ENSP00000263642.2:p.Arg337Gly | |
| NM_022168.3:c.1009A>G | NP_071451.2:p.Arg337Gly | |
| XM_011511628.1:c.292A>G | XP_011509930.1:p.Arg98Gly | |
| XM_011511629.1:c.1009A>G | XP_011509931.1:p.Arg337Gly | |
| NM_022168.4:c.1009A>G MANE Select | NP_071451.2:p.Arg337Gly |