Linked Data
ClinVar Variation Id:
1130997
ClinVar RCV Id:
RCV001464713
dbSNP Id:
rs1792182837
MyVariant Identifiers:
chr7:g.92135584T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92506270T>C , CM000669.2:g.92506270T>C | GRCh38 |
| NC_000007.13:g.92135584T>C , CM000669.1:g.92135584T>C | GRCh37 |
| NC_000007.12:g.91973520T>C | NCBI36 |
| NG_008341.1:g.27262A>G | |
| NG_008341.2:g.27262A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.1878A>G MANE Select | ENSP00000248633.4:p.Arg626= | |
| ENST00000248633.8:c.1878A>G | ENSP00000248633.4:p.Arg626= | |
| ENST00000422866.1:c.696A>G | ||
| ENST00000428214.5:c.1878A>G | ENSP00000394413.1:p.Arg626= | |
| ENST00000438045.5:c.912A>G | ENSP00000410438.1:p.Arg304= | |
| ENST00000484913.5:n.1917A>G | ||
| ENST00000496420.5:n.1554A>G | ||
| NM_000466.2:c.1878A>G | NP_000457.1:p.Arg626= | |
| NM_001282677.1:c.1878A>G | NP_001269606.1:p.Arg626= | |
| NM_001282678.1:c.1254A>G | NP_001269607.1:p.Arg418= | |
| XM_005250433.3:c.129A>G | XP_005250490.1:p.Arg43= | |
| XR_242246.3:n.1974A>G | ||
| XM_017012319.2:c.129A>G | XP_016867808.1:p.Arg43= | |
| XR_001744808.2:n.905A>G | ||
| XR_242246.5:n.1925A>G | ||
| NM_000466.3:c.1878A>G MANE Select | NP_000457.1:p.Arg626= | |
| NM_001282677.2:c.1878A>G | NP_001269606.1:p.Arg626= | |
| NM_001282678.2:c.1254A>G | NP_001269607.1:p.Arg418= |