Linked Data
ClinVar Variation Id:
1600
ClinVar RCV Id:
RCV000001667
dbSNP Id:
rs267606991
ExAC:
1:161046145 C / T
gnomAD v2:
1-161046145-C-T
gnomAD v3:
1-161076355-C-T
gnomAD v4:
1-161076355-C-T
PubMed:
PMID:20691405
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161076355C>T , CM000663.2:g.161076355C>T | GRCh38 |
| NC_000001.10:g.161046145C>T , CM000663.1:g.161046145C>T | GRCh37 |
| NC_000001.9:g.159312769C>T | NCBI36 |
| NG_028109.1:g.18241G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368012.4:c.851G>A MANE Select | ENSP00000356991.3:p.Arg284Gln | |
| ENST00000368012.3:c.851G>A | ENSP00000356991.3:p.Arg284Gln | |
| NM_030916.2:c.851G>A | NP_112178.2:p.Arg284Gln | |
| XM_005245508.2:c.851G>A | XP_005245565.1:p.Arg284Gln | |
| XM_011510021.1:c.851G>A | XP_011508323.1:p.Arg284Gln | |
| XM_011510022.1:c.851G>A | XP_011508324.1:p.Arg284Gln | |
| XM_011510023.1:c.851G>A | XP_011508325.1:p.Arg284Gln | |
| XM_005245508.3:c.851G>A | XP_005245565.1:p.Arg284Gln | |
| XM_011510021.2:c.851G>A | XP_011508323.1:p.Arg284Gln | |
| XM_011510022.2:c.851G>A | XP_011508324.1:p.Arg284Gln | |
| NM_030916.3:c.851G>A MANE Select | NP_112178.2:p.Arg284Gln |