Linked Data
ClinVar Variation Id:
2740539
ClinVar RCV Id:
RCV003589105
dbSNP Id:
rs1566061784
gnomAD v4:
13-23334780-C-A
COSMIC:
COSM378179
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23334780C>A , CM000675.2:g.23334780C>A | GRCh38 |
| NC_000013.10:g.23908919C>A , CM000675.1:g.23908919C>A | GRCh37 |
| NC_000013.9:g.22806919C>A | NCBI36 |
| NG_012342.1:g.103923G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+19005G>T | ENSP00000508399.1:n.2185+19005G>T | |
| ENST00000682944.1:c.9123G>T | ENSP00000507173.1:p.Gln3041His | |
| ENST00000683210.1:c.2185+19005G>T | ENSP00000506739.1:n.2185+19005G>T | |
| ENST00000683270.1:c.6445+2642G>T | ENSP00000507624.1:n.6445+2642G>T | |
| ENST00000683367.1:c.2177-5296G>T | ENSP00000507780.1:n.2177-5296G>T | |
| ENST00000683489.1:c.2292-4828G>T | ENSP00000508403.1:n.2292-4828G>T | |
| ENST00000683680.1:c.2319-4828G>T | ENSP00000507223.1:n.2319-4828G>T | |
| ENST00000684163.1:c.2204-5296G>T | ENSP00000508262.1:n.2204-5296G>T | |
| ENST00000684196.1:n.4543-5296G>T | ||
| ENST00000684325.1:c.2186-13106G>T | ENSP00000508121.1:n.2186-13106G>T | |
| ENST00000684385.1:c.2221-5296G>T | ENSP00000507855.1:n.2221-5296G>T | |
| ENST00000684497.1:c.2186-12136G>T | ENSP00000507057.1:n.2186-12136G>T | |
| ENST00000382292.9:c.9096G>T MANE Select | ENSP00000371729.3:p.Gln3032His | |
| ENST00000423156.2:c.2186-5296G>T | ENSP00000390925.2:n.2186-5296G>T | |
| ENST00000455470.6:c.2432-5296G>T | ENSP00000406565.2:n.2432-5296G>T | |
| ENST00000382292.7:c.9096G>T | ENSP00000371729.3:p.Gln3032His | |
| ENST00000382298.7:c.9096G>T | ENSP00000371735.3:p.Gln3032His | |
| ENST00000402364.1:c.6846G>T | ENSP00000385844.1:p.Gln2282His | |
| ENST00000423156.1:c.1058-5296G>T | ENSP00000390925.1:n.1058-5296G>T | |
| ENST00000455470.5:c.2130-5296G>T | ||
| NM_001278055.1:c.8655G>T | NP_001264984.1:p.Gln2885His | |
| NM_014363.5:c.9096G>T | NP_055178.3:p.Gln3032His | |
| XM_005266338.1:c.9123G>T | XP_005266395.1:p.Gln3041His | |
| XM_011535038.1:c.9147G>T | XP_011533340.1:p.Gln3049His | |
| XM_011535039.1:c.9114G>T | XP_011533341.1:p.Gln3038His | |
| XM_005266338.2:c.9123G>T | XP_005266395.1:p.Gln3041His | |
| XM_011535039.2:c.9114G>T | XP_011533341.1:p.Gln3038His | |
| XM_017020539.1:c.9087G>T | XP_016876028.1:p.Gln3029His | |
| XM_024449337.1:c.9123G>T | XP_024305105.1:p.Gln3041His | |
| NM_014363.6:c.9096G>T MANE Select | NP_055178.3:p.Gln3032His | |
| NM_001278055.2:c.8655G>T | NP_001264984.1:p.Gln2885His |