Linked Data
ClinVar Variation Id:
91496
ClinVar RCV Id:
RCV000077013
RCV000130086
RCV000197898
RCV000656802
RCV001194386
RCV002504987
RCV003460728
dbSNP Id:
rs142899125
ExAC:
13:32936719 A / G
gnomAD v2:
13-32936719-A-G
gnomAD v3:
13-32362582-A-G
gnomAD v4:
13-32362582-A-G
PubMed:
PMID:25085752
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32362582A>G , CM000675.2:g.32362582A>G | GRCh38 |
| NC_000013.10:g.32936719A>G , CM000675.1:g.32936719A>G | GRCh37 |
| NC_000013.9:g.31834719A>G | NCBI36 |
| NG_012772.3:g.52103A>G , LRG_293:g.52103A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.7865A>G | ENSP00000434898.2:p.Asn2622Ser | |
| ENST00000528762.2:c.7865A>G | ENSP00000433168.2:p.Asn2622Ser | |
| ENST00000530893.7:c.7496A>G | ENSP00000499438.2:p.Asn2499Ser | |
| ENST00000665585.2:c.7865A>G | ENSP00000499570.2:p.Asn2622Ser | |
| ENST00000666593.2:c.7865A>G | ENSP00000499256.2:p.Asn2622Ser | |
| ENST00000700202.2:c.7865A>G | ENSP00000514856.2:p.Asn2622Ser | |
| ENST00000700202.1:c.332A>G | ENSP00000514856.1:p.Asn111Ser | |
| ENST00000380152.8:c.7865A>G MANE Select | ENSP00000369497.3:p.Asn2622Ser | |
| ENST00000544455.6:c.7865A>G | ENSP00000439902.1:p.Asn2622Ser | |
| ENST00000614259.2:c.7873A>G | ENSP00000506251.1:p.Ile2625Val | |
| ENST00000665585.1:c.430A>G | ||
| ENST00000680887.1:c.7865A>G | ENSP00000505508.1:p.Asn2622Ser | |
| ENST00000380152.7:c.7865A>G | ENSP00000369497.3:p.Asn2622Ser | |
| ENST00000544455.5:c.7865A>G | ENSP00000439902.1:p.Asn2622Ser | |
| ENST00000614259.1:n.7873A>G | ||
| NM_000059.3:c.7865A>G , LRG_293t1:c.7865A>G | NP_000050.2:p.Asn2622Ser | |
| XM_011535203.1:c.7865A>G | XP_011533505.1:p.Asn2622Ser | |
| XM_011535204.1:c.7769A>G | XP_011533506.1:p.Asn2590Ser | |
| XM_011535205.1:c.7865A>G | XP_011533507.1:p.Asn2622Ser | |
| NM_000059.4:c.7865A>G MANE Select | NP_000050.3:p.Asn2622Ser |