Linked Data
ClinVar Variation Id:
15058
ClinVar RCV Id:
RCV000016205
dbSNP Id:
rs34389944
gnomAD v3:
11-5234357-C-T
gnomAD v4:
11-5234357-C-T
PubMed:
PMID:3841531
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5234357C>T , CM000673.2:g.5234357C>T | GRCh38 |
| NC_000011.9:g.5255587C>T , CM000673.1:g.5255587C>T | GRCh37 |
| NC_000011.8:g.5212163C>T | NCBI36 |
| NG_000007.3:g.63259G>A | |
| NG_063112.2:g.14301G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000643122.1:c.77G>A | ENSP00000494708.1:p.Gly26Asp | |
| ENST00000650601.1:c.77G>A MANE Select | ENSP00000497529.1:p.Gly26Asp | |
| ENST00000292901.7:c.77G>A | ENSP00000292901.3:p.Gly26Asp | |
| ENST00000380299.3:c.77G>A | ENSP00000369654.3:p.Gly26Asp | |
| ENST00000417377.1:c.77G>A | ENSP00000414741.1:p.Gly26Asp | |
| ENST00000429817.1:c.77G>A | ENSP00000393810.1:p.Gly26Asp | |
| NM_000519.3:c.77G>A | NP_000510.1:p.Gly26Asp | |
| NM_000519.4:c.77G>A MANE Select | NP_000510.1:p.Gly26Asp |