Linked Data
ClinVar Variation Id:
391872
ClinVar RCV Id:
RCV000441442
dbSNP Id:
rs746834684
gnomAD v4:
13-23334977-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23334977G>T , CM000675.2:g.23334977G>T | GRCh38 |
| NC_000013.10:g.23909116G>T , CM000675.1:g.23909116G>T | GRCh37 |
| NC_000013.9:g.22807116G>T | NCBI36 |
| NG_012342.1:g.103726C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682775.1:c.2185+18808C>A | ENSP00000508399.1:n.2185+18808C>A | |
| ENST00000682944.1:c.8926C>A | ENSP00000507173.1:p.Arg2976Ser | |
| ENST00000683210.1:c.2185+18808C>A | ENSP00000506739.1:n.2185+18808C>A | |
| ENST00000683270.1:c.6445+2445C>A | ENSP00000507624.1:n.6445+2445C>A | |
| ENST00000683367.1:c.2177-5493C>A | ENSP00000507780.1:n.2177-5493C>A | |
| ENST00000683489.1:c.2292-5025C>A | ENSP00000508403.1:n.2292-5025C>A | |
| ENST00000683680.1:c.2319-5025C>A | ENSP00000507223.1:n.2319-5025C>A | |
| ENST00000684163.1:c.2204-5493C>A | ENSP00000508262.1:n.2204-5493C>A | |
| ENST00000684196.1:n.4543-5493C>A | ||
| ENST00000684325.1:c.2186-13303C>A | ENSP00000508121.1:n.2186-13303C>A | |
| ENST00000684385.1:c.2221-5493C>A | ENSP00000507855.1:n.2221-5493C>A | |
| ENST00000684497.1:c.2186-12333C>A | ENSP00000507057.1:n.2186-12333C>A | |
| ENST00000382292.9:c.8899C>A MANE Select | ENSP00000371729.3:p.Arg2967Ser | |
| ENST00000423156.2:c.2186-5493C>A | ENSP00000390925.2:n.2186-5493C>A | |
| ENST00000455470.6:c.2432-5493C>A | ENSP00000406565.2:n.2432-5493C>A | |
| ENST00000382292.7:c.8899C>A | ENSP00000371729.3:p.Arg2967Ser | |
| ENST00000382298.7:c.8899C>A | ENSP00000371735.3:p.Arg2967Ser | |
| ENST00000402364.1:c.6649C>A | ENSP00000385844.1:p.Arg2217Ser | |
| ENST00000423156.1:c.1058-5493C>A | ENSP00000390925.1:n.1058-5493C>A | |
| ENST00000455470.5:c.2130-5493C>A | ||
| NM_001278055.1:c.8458C>A | NP_001264984.1:p.Arg2820Ser | |
| NM_014363.5:c.8899C>A | NP_055178.3:p.Arg2967Ser | |
| XM_005266338.1:c.8926C>A | XP_005266395.1:p.Arg2976Ser | |
| XM_011535038.1:c.8950C>A | XP_011533340.1:p.Arg2984Ser | |
| XM_011535039.1:c.8917C>A | XP_011533341.1:p.Arg2973Ser | |
| XM_005266338.2:c.8926C>A | XP_005266395.1:p.Arg2976Ser | |
| XM_011535039.2:c.8917C>A | XP_011533341.1:p.Arg2973Ser | |
| XM_017020539.1:c.8890C>A | XP_016876028.1:p.Arg2964Ser | |
| XM_024449337.1:c.8926C>A | XP_024305105.1:p.Arg2976Ser | |
| NM_014363.6:c.8899C>A MANE Select | NP_055178.3:p.Arg2967Ser | |
| NM_001278055.2:c.8458C>A | NP_001264984.1:p.Arg2820Ser |