Linked Data
ClinVar Variation Id:
1554894
ClinVar RCV Id:
RCV002192569
dbSNP Id:
rs146715254
gnomAD v2:
17-40695821-C-T
gnomAD v4:
17-42543803-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543803C>T , CM000679.2:g.42543803C>T | GRCh38 |
| NC_000017.10:g.40695821C>T , CM000679.1:g.40695821C>T | GRCh37 |
| NC_000017.9:g.37949347C>T | NCBI36 |
| NG_011552.1:g.12871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1797C>T MANE Select | ENSP00000225927.1:p.Ala599= | |
| ENST00000225927.6:c.1797C>T | ENSP00000225927.1:p.Ala599= | |
| ENST00000591587.1:c.1135C>T | ENSP00000467836.1:n.1135C>T | |
| NM_000263.3:c.1797C>T | NP_000254.2:p.Ala599= | |
| XM_006721920.2:c.966C>T | XP_006721983.1:p.Ala322= | |
| XM_011524840.1:c.798C>T | XP_011523142.1:p.Ala266= | |
| XM_017024687.1:c.966C>T | XP_016880176.1:p.Ala322= | |
| XM_024450771.1:c.1854C>T | XP_024306539.1:p.Ala618= | |
| XM_024450772.1:c.798C>T | XP_024306540.1:p.Ala266= | |
| NM_000263.4:c.1797C>T MANE Select | NP_000254.2:p.Ala599= |