Linked Data
ClinVar Variation Id:
24470
ClinVar RCV Id:
RCV000021349
dbSNP Id:
rs104886153
PubMed:
PMID:17396119
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108601441G>A , CM000685.2:g.108601441G>A | GRCh38 |
| NC_000023.10:g.107844671G>A , CM000685.1:g.107844671G>A | GRCh37 |
| NC_000023.9:g.107731327G>A | NCBI36 |
| NG_011977.1:g.166518G>A | |
| NG_011977.2:g.166518G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.1997G>A MANE Select | ENSP00000331902.7:p.Gly666Asp | |
| ENST00000361603.7:c.1997G>A | ENSP00000354505.2:p.Gly666Asp | |
| ENST00000328300.10:c.1997G>A | ENSP00000331902.6:p.Gly666Asp | |
| ENST00000361603.6:c.1997G>A | ENSP00000354505.2:p.Gly666Asp | |
| ENST00000483338.1:n.1453G>A | ||
| NM_000495.4:c.1997G>A | NP_000486.1:p.Gly666Asp | |
| NM_033380.2:c.1997G>A | NP_203699.1:p.Gly666Asp | |
| XM_005262070.2:c.1997G>A | XP_005262127.1:p.Gly666Asp | |
| XM_005262072.3:c.1997G>A | XP_005262129.1:p.Gly666Asp | |
| XM_006724616.2:c.1997G>A | XP_006724679.1:p.Gly666Asp | |
| XM_011530849.1:c.1673G>A | XP_011529151.1:p.Gly558Asp | |
| XM_011530850.1:c.1997G>A | XP_011529152.1:p.Gly666Asp | |
| XM_011530849.2:c.2012G>A | XP_011529151.2:p.Gly671Asp | |
| XM_017029259.2:c.2012G>A | XP_016884748.1:p.Gly671Asp | |
| XM_017029260.1:c.2012G>A | XP_016884749.1:p.Gly671Asp | |
| XM_017029261.1:c.2012G>A | XP_016884750.1:p.Gly671Asp | |
| XM_017029262.2:c.2012G>A | XP_016884751.1:p.Gly671Asp | |
| XM_017029263.2:c.332G>A | XP_016884752.1:p.Gly111Asp | |
| NM_000495.5:c.1997G>A | NP_000486.1:p.Gly666Asp | |
| NM_033380.3:c.1997G>A MANE Select | NP_203699.1:p.Gly666Asp |