Linked Data
ClinVar Variation Id:
66984
dbSNP Id:
rs397515485
gnomAD v4:
X-153964283-G-A
PubMed:
PMID:24011988
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153964283G>A , CM000685.2:g.153964283G>A | GRCh38 |
| NC_000023.10:g.153229734G>A , CM000685.1:g.153229734G>A | GRCh37 |
| NC_000023.9:g.152882928G>A | NCBI36 |
| NG_012513.1:g.12086C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310441.12:c.344C>T MANE Select | ENSP00000309555.7:p.Ala115Val | |
| ENST00000310441.11:c.344C>T | ENSP00000309555.7:p.Ala115Val | |
| ENST00000369984.4:c.344C>T | ENSP00000359001.4:p.Ala115Val | |
| NM_005334.2:c.344C>T | NP_005325.2:p.Ala115Val | |
| XM_006724815.1:c.344C>T | XP_006724878.1:p.Ala115Val | |
| XM_006724816.1:c.344C>T | XP_006724879.1:p.Ala115Val | |
| XM_011531144.1:c.344C>T | XP_011529446.1:p.Ala115Val | |
| XM_011531145.1:c.344C>T | XP_011529447.1:p.Ala115Val | |
| XM_011531146.1:c.344C>T | XP_011529448.1:p.Ala115Val | |
| XM_011531147.1:c.344C>T | XP_011529449.1:p.Ala115Val | |
| XM_011531148.1:c.344C>T | XP_011529450.1:p.Ala115Val | |
| XM_011531149.1:c.344C>T | XP_011529451.1:p.Ala115Val | |
| XM_006724815.3:c.344C>T | XP_006724878.1:p.Ala115Val | |
| XM_006724816.3:c.344C>T | XP_006724879.1:p.Ala115Val | |
| XM_011531147.3:c.344C>T | XP_011529449.1:p.Ala115Val | |
| XM_011531148.3:c.344C>T | XP_011529450.1:p.Ala115Val | |
| XM_017029471.2:c.344C>T | XP_016884960.1:p.Ala115Val | |
| NM_005334.3:c.344C>T MANE Select | NP_005325.2:p.Ala115Val |