Linked Data
ClinVar Variation Id:
24880
ClinVar RCV Id:
RCV000034779
RCV000121992
RCV000276548
RCV000333869
RCV000354891
RCV000367517
RCV000565970
RCV000755685
RCV001083006
RCV003492298
dbSNP Id:
rs34682185
ExAC:
10:43601830 G / A
gnomAD v2:
10-43601830-G-A
gnomAD v3:
10-43106382-G-A
gnomAD v4:
10-43106382-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43106382G>A , CM000672.2:g.43106382G>A | GRCh38 |
| NC_000010.10:g.43601830G>A , CM000672.1:g.43601830G>A | GRCh37 |
| NC_000010.9:g.42921836G>A | NCBI36 |
| NG_007489.1:g.34314G>A , LRG_518:g.34314G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.867+1189G>A | ENSP00000480088.2:n.867+1189G>A | |
| ENST00000683007.1:n.448G>A | ||
| ENST00000340058.6:c.874G>A | ENSP00000344798.4:p.Val292Met | |
| ENST00000355710.8:c.874G>A MANE Select | ENSP00000347942.3:p.Val292Met | |
| ENST00000671844.1:c.625+3753G>A | ENSP00000500541.1:n.625+3753G>A | |
| ENST00000672389.1:c.74-4825G>A | ENSP00000500252.1:n.74-4825G>A | |
| ENST00000340058.5:c.874G>A | ENSP00000344798.4:p.Val292Met | |
| ENST00000355710.7:c.874G>A | ENSP00000347942.3:p.Val292Met | |
| ENST00000479913.1:n.469G>A | ||
| ENST00000498820.5:c.74-5717G>A | ENSP00000419080.1:n.74-5717G>A | |
| ENST00000615310.4:c.874G>A | ENSP00000480088.1:p.Val292Met | |
| NM_020630.4:c.874G>A , LRG_518t2:c.874G>A | NP_065681.1:p.Val292Met | |
| NM_020975.4:c.874G>A , LRG_518t1:c.874G>A | NP_066124.1:p.Val292Met | |
| XM_011540027.1:c.874G>A | XP_011538329.1:p.Val292Met | |
| NM_001355216.1:c.112G>A | NP_001342145.1:p.Val38Met | |
| NM_020630.5:c.874G>A | NP_065681.1:p.Val292Met | |
| NM_020975.5:c.874G>A | NP_066124.1:p.Val292Met | |
| NM_020975.6:c.874G>A MANE Select | NP_066124.1:p.Val292Met | |
| NM_020630.6:c.874G>A | NP_065681.1:p.Val292Met |