Linked Data
ClinVar Variation Id:
1145040
ClinVar RCV Id:
RCV001483733
dbSNP Id:
rs1304752867
gnomAD v4:
13-23330172-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23330172T>G , CM000675.2:g.23330172T>G | GRCh38 |
| NC_000013.10:g.23904311T>G , CM000675.1:g.23904311T>G | GRCh37 |
| NC_000013.9:g.22802311T>G | NCBI36 |
| NG_012342.1:g.108531A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2186-18057A>C | ENSP00000508399.1:n.2186-18057A>C | |
| ENST00000682944.1:c.13731A>C | ENSP00000507173.1:p.Ile4577= | |
| ENST00000683210.1:c.2185+23613A>C | ENSP00000506739.1:n.2185+23613A>C | |
| ENST00000683270.1:c.6446-688A>C | ENSP00000507624.1:n.6446-688A>C | |
| ENST00000683367.1:c.2177-688A>C | ENSP00000507780.1:n.2177-688A>C | |
| ENST00000683489.1:c.2292-220A>C | ENSP00000508403.1:n.2292-220A>C | |
| ENST00000683680.1:c.2319-220A>C | ENSP00000507223.1:n.2319-220A>C | |
| ENST00000684163.1:c.2204-688A>C | ENSP00000508262.1:n.2204-688A>C | |
| ENST00000684196.1:n.4543-688A>C | ||
| ENST00000684325.1:c.2186-8498A>C | ENSP00000508121.1:n.2186-8498A>C | |
| ENST00000684385.1:c.2221-688A>C | ENSP00000507855.1:n.2221-688A>C | |
| ENST00000684497.1:c.2186-7528A>C | ENSP00000507057.1:n.2186-7528A>C | |
| ENST00000382292.9:c.13704A>C MANE Select | ENSP00000371729.3:p.Ile4568= | |
| ENST00000423156.2:c.2186-688A>C | ENSP00000390925.2:n.2186-688A>C | |
| ENST00000455470.6:c.2432-688A>C | ENSP00000406565.2:n.2432-688A>C | |
| ENST00000382292.7:c.13704A>C | ENSP00000371729.3:p.Ile4568= | |
| ENST00000382298.7:c.13704A>C | ENSP00000371735.3:p.Ile4568= | |
| ENST00000402364.1:c.11454A>C | ENSP00000385844.1:p.Ile3818= | |
| ENST00000423156.1:c.1058-688A>C | ENSP00000390925.1:n.1058-688A>C | |
| ENST00000455470.5:c.2130-688A>C | ||
| NM_001278055.1:c.13263A>C | NP_001264984.1:p.Ile4421= | |
| NM_014363.5:c.13704A>C | NP_055178.3:p.Ile4568= | |
| XM_005266338.1:c.13731A>C | XP_005266395.1:p.Ile4577= | |
| XM_011535038.1:c.13755A>C | XP_011533340.1:p.Ile4585= | |
| XM_011535039.1:c.13722A>C | XP_011533341.1:p.Ile4574= | |
| XM_005266338.2:c.13731A>C | XP_005266395.1:p.Ile4577= | |
| XM_011535039.2:c.13722A>C | XP_011533341.1:p.Ile4574= | |
| XM_017020539.1:c.13695A>C | XP_016876028.1:p.Ile4565= | |
| XM_024449337.1:c.13731A>C | XP_024305105.1:p.Ile4577= | |
| NM_014363.6:c.13704A>C MANE Select | NP_055178.3:p.Ile4568= | |
| NM_001278055.2:c.13263A>C | NP_001264984.1:p.Ile4421= |