Linked Data
ClinVar Variation Id:
2695736
ClinVar RCV Id:
RCV003530376
dbSNP Id:
rs2137613547
MyVariant Identifiers:
chr13:g.32950925T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32376788T>A , CM000675.2:g.32376788T>A | GRCh38 |
| NC_000013.10:g.32950925T>A , CM000675.1:g.32950925T>A | GRCh37 |
| NC_000013.9:g.31848925T>A | NCBI36 |
| NG_012772.3:g.66309T>A , LRG_293:g.66309T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.8751T>A | ENSP00000434898.2:p.Leu2917= | |
| ENST00000528762.2:c.*118T>A | ENSP00000433168.2:n.*118T>A | |
| ENST00000530893.7:c.8382T>A | ENSP00000499438.2:p.Leu2794= | |
| ENST00000665585.2:c.*313T>A | ENSP00000499570.2:n.*313T>A | |
| ENST00000666593.2:c.8751T>A | ENSP00000499256.2:p.Leu2917= | |
| ENST00000700202.2:c.8751T>A | ENSP00000514856.2:p.Leu2917= | |
| ENST00000700202.1:c.1218T>A | ENSP00000514856.1:p.Leu406= | |
| ENST00000700203.1:n.878T>A | ||
| ENST00000380152.8:c.8751T>A MANE Select | ENSP00000369497.3:p.Leu2917= | |
| ENST00000544455.6:c.8751T>A | ENSP00000439902.1:p.Leu2917= | |
| ENST00000614259.2:c.8759T>A | ENSP00000506251.1:n.8759T>A | |
| ENST00000665585.1:c.1629T>A | ||
| ENST00000680887.1:c.8751T>A | ENSP00000505508.1:p.Leu2917= | |
| ENST00000380152.7:c.8751T>A | ENSP00000369497.3:p.Leu2917= | |
| ENST00000528762.1:c.313T>A | ENSP00000433168.1:n.313T>A | |
| ENST00000544455.5:c.8751T>A | ENSP00000439902.1:p.Leu2917= | |
| NM_000059.3:c.8751T>A , LRG_293t1:c.8751T>A | NP_000050.2:p.Leu2917= | |
| XM_011535203.1:c.8751T>A | XP_011533505.1:p.Leu2917= | |
| XM_011535204.1:c.8655T>A | XP_011533506.1:p.Leu2885= | |
| XM_011535205.1:c.8751T>A | XP_011533507.1:p.Leu2917= | |
| NM_000059.4:c.8751T>A MANE Select | NP_000050.3:p.Leu2917= |