Linked Data
ClinVar Variation Id:
2809098
ClinVar RCV Id:
RCV003751713
dbSNP Id:
rs769198115
ExAC:
13:23904415 A / G
gnomAD v3:
13-23330276-A-G
gnomAD v4:
13-23330276-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23330276A>G , CM000675.2:g.23330276A>G | GRCh38 |
| NC_000013.10:g.23904415A>G , CM000675.1:g.23904415A>G | GRCh37 |
| NC_000013.9:g.22802415A>G | NCBI36 |
| NG_012342.1:g.108427T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2186-18161T>C | ENSP00000508399.1:n.2186-18161T>C | |
| ENST00000682944.1:c.13627T>C | ENSP00000507173.1:p.Leu4543= | |
| ENST00000683210.1:c.2185+23509T>C | ENSP00000506739.1:n.2185+23509T>C | |
| ENST00000683270.1:c.6446-792T>C | ENSP00000507624.1:n.6446-792T>C | |
| ENST00000683367.1:c.2177-792T>C | ENSP00000507780.1:n.2177-792T>C | |
| ENST00000683489.1:c.2292-324T>C | ENSP00000508403.1:n.2292-324T>C | |
| ENST00000683680.1:c.2319-324T>C | ENSP00000507223.1:n.2319-324T>C | |
| ENST00000684163.1:c.2204-792T>C | ENSP00000508262.1:n.2204-792T>C | |
| ENST00000684196.1:n.4543-792T>C | ||
| ENST00000684325.1:c.2186-8602T>C | ENSP00000508121.1:n.2186-8602T>C | |
| ENST00000684385.1:c.2221-792T>C | ENSP00000507855.1:n.2221-792T>C | |
| ENST00000684497.1:c.2186-7632T>C | ENSP00000507057.1:n.2186-7632T>C | |
| ENST00000382292.9:c.13600T>C MANE Select | ENSP00000371729.3:p.Leu4534= | |
| ENST00000423156.2:c.2186-792T>C | ENSP00000390925.2:n.2186-792T>C | |
| ENST00000455470.6:c.2432-792T>C | ENSP00000406565.2:n.2432-792T>C | |
| ENST00000382292.7:c.13600T>C | ENSP00000371729.3:p.Leu4534= | |
| ENST00000382298.7:c.13600T>C | ENSP00000371735.3:p.Leu4534= | |
| ENST00000402364.1:c.11350T>C | ENSP00000385844.1:p.Leu3784= | |
| ENST00000423156.1:c.1058-792T>C | ENSP00000390925.1:n.1058-792T>C | |
| ENST00000455470.5:c.2130-792T>C | ||
| NM_001278055.1:c.13159T>C | NP_001264984.1:p.Leu4387= | |
| NM_014363.5:c.13600T>C | NP_055178.3:p.Leu4534= | |
| XM_005266338.1:c.13627T>C | XP_005266395.1:p.Leu4543= | |
| XM_011535038.1:c.13651T>C | XP_011533340.1:p.Leu4551= | |
| XM_011535039.1:c.13618T>C | XP_011533341.1:p.Leu4540= | |
| XM_005266338.2:c.13627T>C | XP_005266395.1:p.Leu4543= | |
| XM_011535039.2:c.13618T>C | XP_011533341.1:p.Leu4540= | |
| XM_017020539.1:c.13591T>C | XP_016876028.1:p.Leu4531= | |
| XM_024449337.1:c.13627T>C | XP_024305105.1:p.Leu4543= | |
| NM_014363.6:c.13600T>C MANE Select | NP_055178.3:p.Leu4534= | |
| NM_001278055.2:c.13159T>C | NP_001264984.1:p.Leu4387= |