Linked Data
ClinVar Variation Id:
1620256
ClinVar RCV Id:
RCV002089333
dbSNP Id:
rs2137574942
gnomAD v4:
13-23333448-T-C
MyVariant Identifiers:
chr13:g.23907587T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23333448T>C , CM000675.2:g.23333448T>C | GRCh38 |
| NC_000013.10:g.23907587T>C , CM000675.1:g.23907587T>C | GRCh37 |
| NC_000013.9:g.22805587T>C | NCBI36 |
| NG_012342.1:g.105255A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+20337A>G | ENSP00000508399.1:n.2185+20337A>G | |
| ENST00000682944.1:c.10455A>G | ENSP00000507173.1:p.Val3485= | |
| ENST00000683210.1:c.2185+20337A>G | ENSP00000506739.1:n.2185+20337A>G | |
| ENST00000683270.1:c.6446-3964A>G | ENSP00000507624.1:n.6446-3964A>G | |
| ENST00000683367.1:c.2177-3964A>G | ENSP00000507780.1:n.2177-3964A>G | |
| ENST00000683489.1:c.2292-3496A>G | ENSP00000508403.1:n.2292-3496A>G | |
| ENST00000683680.1:c.2319-3496A>G | ENSP00000507223.1:n.2319-3496A>G | |
| ENST00000684163.1:c.2204-3964A>G | ENSP00000508262.1:n.2204-3964A>G | |
| ENST00000684196.1:n.4543-3964A>G | ||
| ENST00000684325.1:c.2186-11774A>G | ENSP00000508121.1:n.2186-11774A>G | |
| ENST00000684385.1:c.2221-3964A>G | ENSP00000507855.1:n.2221-3964A>G | |
| ENST00000684497.1:c.2186-10804A>G | ENSP00000507057.1:n.2186-10804A>G | |
| ENST00000382292.9:c.10428A>G MANE Select | ENSP00000371729.3:p.Val3476= | |
| ENST00000423156.2:c.2186-3964A>G | ENSP00000390925.2:n.2186-3964A>G | |
| ENST00000455470.6:c.2432-3964A>G | ENSP00000406565.2:n.2432-3964A>G | |
| ENST00000382292.7:c.10428A>G | ENSP00000371729.3:p.Val3476= | |
| ENST00000382298.7:c.10428A>G | ENSP00000371735.3:p.Val3476= | |
| ENST00000402364.1:c.8178A>G | ENSP00000385844.1:p.Val2726= | |
| ENST00000423156.1:c.1058-3964A>G | ENSP00000390925.1:n.1058-3964A>G | |
| ENST00000455470.5:c.2130-3964A>G | ||
| NM_001278055.1:c.9987A>G | NP_001264984.1:p.Val3329= | |
| NM_014363.5:c.10428A>G | NP_055178.3:p.Val3476= | |
| XM_005266338.1:c.10455A>G | XP_005266395.1:p.Val3485= | |
| XM_011535038.1:c.10479A>G | XP_011533340.1:p.Val3493= | |
| XM_011535039.1:c.10446A>G | XP_011533341.1:p.Val3482= | |
| XM_005266338.2:c.10455A>G | XP_005266395.1:p.Val3485= | |
| XM_011535039.2:c.10446A>G | XP_011533341.1:p.Val3482= | |
| XM_017020539.1:c.10419A>G | XP_016876028.1:p.Val3473= | |
| XM_024449337.1:c.10455A>G | XP_024305105.1:p.Val3485= | |
| NM_014363.6:c.10428A>G MANE Select | NP_055178.3:p.Val3476= | |
| NM_001278055.2:c.9987A>G | NP_001264984.1:p.Val3329= |