Linked Data
ClinVar Variation Id:
1099763
ClinVar RCV Id:
RCV001422165
dbSNP Id:
rs2092913790
MyVariant Identifiers:
chr17:g.40690711C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42538693C>T , CM000679.2:g.42538693C>T | GRCh38 |
| NC_000017.10:g.40690711C>T , CM000679.1:g.40690711C>T | GRCh37 |
| NC_000017.9:g.37944237C>T | NCBI36 |
| NG_011552.1:g.7761C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000225927.7:c.702C>T MANE Select | ENSP00000225927.1:p.Arg234= | |
| ENST00000225927.6:c.702C>T | ENSP00000225927.1:p.Arg234= | |
| ENST00000586516.5:c.304C>T | ||
| ENST00000591587.1:c.297C>T | ENSP00000467836.1:p.Arg99= | |
| NM_000263.3:c.702C>T | NP_000254.2:p.Arg234= | |
| XM_006721920.2:c.-41C>T | XP_006721983.1:n.-41C>T | |
| XM_011524840.1:c.-41C>T | XP_011523142.1:n.-41C>T | |
| XM_017024687.1:c.-41C>T | XP_016880176.1:n.-41C>T | |
| XM_024450771.1:c.759C>T | XP_024306539.1:p.Arg253= | |
| XM_024450772.1:c.-41C>T | XP_024306540.1:n.-41C>T | |
| NM_000263.4:c.702C>T MANE Select | NP_000254.2:p.Arg234= |