Linked Data
ClinVar Variation Id:
448211
dbSNP Id:
rs769751841
ExAC:
13:23911985 C / A
gnomAD v2:
13-23911985-C-A
gnomAD v3:
13-23337846-C-A
gnomAD v4:
13-23337846-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23337846C>A , CM000675.2:g.23337846C>A | GRCh38 |
| NC_000013.10:g.23911985C>A , CM000675.1:g.23911985C>A | GRCh37 |
| NC_000013.9:g.22809985C>A | NCBI36 |
| NG_012342.1:g.100857G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+15939G>T | ENSP00000508399.1:n.2185+15939G>T | |
| ENST00000682944.1:c.6057G>T | ENSP00000507173.1:p.Lys2019Asn | |
| ENST00000683210.1:c.2185+15939G>T | ENSP00000506739.1:n.2185+15939G>T | |
| ENST00000683270.1:c.6021G>T | ENSP00000507624.1:p.Lys2007Asn | |
| ENST00000683367.1:c.2177-8362G>T | ENSP00000507780.1:n.2177-8362G>T | |
| ENST00000683489.1:c.2291+3739G>T | ENSP00000508403.1:n.2291+3739G>T | |
| ENST00000683680.1:c.2318+3739G>T | ENSP00000507223.1:n.2318+3739G>T | |
| ENST00000684163.1:c.2204-8362G>T | ENSP00000508262.1:n.2204-8362G>T | |
| ENST00000684196.1:n.4543-8362G>T | ||
| ENST00000684325.1:c.2185+15939G>T | ENSP00000508121.1:n.2185+15939G>T | |
| ENST00000684385.1:c.2221-8362G>T | ENSP00000507855.1:n.2221-8362G>T | |
| ENST00000684497.1:c.2186-15202G>T | ENSP00000507057.1:n.2186-15202G>T | |
| ENST00000382292.9:c.6030G>T MANE Select | ENSP00000371729.3:p.Lys2010Asn | |
| ENST00000423156.2:c.2186-8362G>T | ENSP00000390925.2:n.2186-8362G>T | |
| ENST00000455470.6:c.2431+3599G>T | ENSP00000406565.2:n.2431+3599G>T | |
| ENST00000382292.7:c.6030G>T | ENSP00000371729.3:p.Lys2010Asn | |
| ENST00000382298.7:c.6030G>T | ENSP00000371735.3:p.Lys2010Asn | |
| ENST00000402364.1:c.3780G>T | ENSP00000385844.1:p.Lys1260Asn | |
| ENST00000423156.1:c.1058-8362G>T | ENSP00000390925.1:n.1058-8362G>T | |
| ENST00000455470.5:c.2129+3599G>T | ||
| NM_001278055.1:c.5589G>T | NP_001264984.1:p.Lys1863Asn | |
| NM_014363.5:c.6030G>T | NP_055178.3:p.Lys2010Asn | |
| XM_005266338.1:c.6057G>T | XP_005266395.1:p.Lys2019Asn | |
| XM_011535038.1:c.6081G>T | XP_011533340.1:p.Lys2027Asn | |
| XM_011535039.1:c.6048G>T | XP_011533341.1:p.Lys2016Asn | |
| XM_005266338.2:c.6057G>T | XP_005266395.1:p.Lys2019Asn | |
| XM_011535039.2:c.6048G>T | XP_011533341.1:p.Lys2016Asn | |
| XM_017020539.1:c.6021G>T | XP_016876028.1:p.Lys2007Asn | |
| XM_024449337.1:c.6057G>T | XP_024305105.1:p.Lys2019Asn | |
| NM_014363.6:c.6030G>T MANE Select | NP_055178.3:p.Lys2010Asn | |
| NM_001278055.2:c.5589G>T | NP_001264984.1:p.Lys1863Asn |