Linked Data
ClinVar Variation Id:
524941
ClinVar RCV Id:
RCV000628843
dbSNP Id:
rs1173357672
gnomAD v2:
11-47372877-G-A
gnomAD v3:
11-47351326-G-A
gnomAD v4:
11-47351326-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47351326G>A , CM000673.2:g.47351326G>A | GRCh38 |
| NC_000011.9:g.47372877G>A , CM000673.1:g.47372877G>A | GRCh37 |
| NC_000011.8:g.47329453G>A | NCBI36 |
| NG_007667.1:g.6377C>T , LRG_386:g.6377C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.205C>T MANE Select | ENSP00000442795.1:p.Arg69Trp | |
| ENST00000256993.8:c.205C>T | ENSP00000256993.5:p.Arg69Trp | |
| ENST00000399249.6:c.205C>T | ENSP00000382193.2:p.Arg69Trp | |
| ENST00000544791.1:c.205C>T | ENSP00000444259.1:p.Arg69Trp | |
| ENST00000545968.5:c.205C>T | ENSP00000442795.1:p.Arg69Trp | |
| NM_000256.3:c.205C>T , LRG_386t1:c.205C>T MANE Select | NP_000247.2:p.Arg69Trp | |
| XM_011520117.1:c.205C>T | XP_011518419.1:p.Arg69Trp | |
| XM_011520118.1:c.205C>T | XP_011518420.1:p.Arg69Trp |