Linked Data
ClinVar Variation Id:
1528450
ClinVar RCV Id:
RCV002071266
dbSNP Id:
rs2137586583
MyVariant Identifiers:
chr13:g.23908892T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23334753T>C , CM000675.2:g.23334753T>C | GRCh38 |
| NC_000013.10:g.23908892T>C , CM000675.1:g.23908892T>C | GRCh37 |
| NC_000013.9:g.22806892T>C | NCBI36 |
| NG_012342.1:g.103950A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+19032A>G | ENSP00000508399.1:n.2185+19032A>G | |
| ENST00000682944.1:c.9150A>G | ENSP00000507173.1:p.Ala3050= | |
| ENST00000683210.1:c.2185+19032A>G | ENSP00000506739.1:n.2185+19032A>G | |
| ENST00000683270.1:c.6445+2669A>G | ENSP00000507624.1:n.6445+2669A>G | |
| ENST00000683367.1:c.2177-5269A>G | ENSP00000507780.1:n.2177-5269A>G | |
| ENST00000683489.1:c.2292-4801A>G | ENSP00000508403.1:n.2292-4801A>G | |
| ENST00000683680.1:c.2319-4801A>G | ENSP00000507223.1:n.2319-4801A>G | |
| ENST00000684163.1:c.2204-5269A>G | ENSP00000508262.1:n.2204-5269A>G | |
| ENST00000684196.1:n.4543-5269A>G | ||
| ENST00000684325.1:c.2186-13079A>G | ENSP00000508121.1:n.2186-13079A>G | |
| ENST00000684385.1:c.2221-5269A>G | ENSP00000507855.1:n.2221-5269A>G | |
| ENST00000684497.1:c.2186-12109A>G | ENSP00000507057.1:n.2186-12109A>G | |
| ENST00000382292.9:c.9123A>G MANE Select | ENSP00000371729.3:p.Ala3041= | |
| ENST00000423156.2:c.2186-5269A>G | ENSP00000390925.2:n.2186-5269A>G | |
| ENST00000455470.6:c.2432-5269A>G | ENSP00000406565.2:n.2432-5269A>G | |
| ENST00000382292.7:c.9123A>G | ENSP00000371729.3:p.Ala3041= | |
| ENST00000382298.7:c.9123A>G | ENSP00000371735.3:p.Ala3041= | |
| ENST00000402364.1:c.6873A>G | ENSP00000385844.1:p.Ala2291= | |
| ENST00000423156.1:c.1058-5269A>G | ENSP00000390925.1:n.1058-5269A>G | |
| ENST00000455470.5:c.2130-5269A>G | ||
| NM_001278055.1:c.8682A>G | NP_001264984.1:p.Ala2894= | |
| NM_014363.5:c.9123A>G | NP_055178.3:p.Ala3041= | |
| XM_005266338.1:c.9150A>G | XP_005266395.1:p.Ala3050= | |
| XM_011535038.1:c.9174A>G | XP_011533340.1:p.Ala3058= | |
| XM_011535039.1:c.9141A>G | XP_011533341.1:p.Ala3047= | |
| XM_005266338.2:c.9150A>G | XP_005266395.1:p.Ala3050= | |
| XM_011535039.2:c.9141A>G | XP_011533341.1:p.Ala3047= | |
| XM_017020539.1:c.9114A>G | XP_016876028.1:p.Ala3038= | |
| XM_024449337.1:c.9150A>G | XP_024305105.1:p.Ala3050= | |
| NM_014363.6:c.9123A>G MANE Select | NP_055178.3:p.Ala3041= | |
| NM_001278055.2:c.8682A>G | NP_001264984.1:p.Ala2894= |