Linked Data
ClinVar Variation Id:
185797
ClinVar RCV Id:
RCV000165286
dbSNP Id:
rs786202465
gnomAD v4:
16-68738369-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68738369G>A , CM000678.2:g.68738369G>A | GRCh38 |
| NC_000016.9:g.68772272G>A , CM000678.1:g.68772272G>A | GRCh37 |
| NC_000016.8:g.67329773G>A | NCBI36 |
| NG_008021.1:g.6078G>A , LRG_301:g.6078G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.121G>A MANE Select | ENSP00000261769.4:p.Val41Met | |
| ENST00000261769.9:c.121G>A | ENSP00000261769.4:p.Val41Met | |
| ENST00000422392.6:c.121G>A | ENSP00000414946.2:p.Val41Met | |
| ENST00000566510.5:c.121G>A | ENSP00000458139.1:p.Val41Met | |
| ENST00000566612.5:c.121G>A | ENSP00000454782.1:p.Val41Met | |
| ENST00000611625.4:c.121G>A | ENSP00000481063.1:p.Val41Met | |
| ENST00000612417.4:c.121G>A | ENSP00000478360.1:p.Val41Met | |
| ENST00000621016.4:c.121G>A | ENSP00000480664.1:p.Val41Met | |
| NM_004360.3:c.121G>A , LRG_301t1:c.121G>A | NP_004351.1:p.Val41Met | |
| NM_001317184.1:c.121G>A | NP_001304113.1:p.Val41Met | |
| NM_001317185.1:c.-1495G>A | NP_001304114.1:n.-1495G>A | |
| NM_001317186.1:c.-1699G>A | NP_001304115.1:n.-1699G>A | |
| NM_004360.4:c.121G>A | NP_004351.1:p.Val41Met | |
| NM_004360.5:c.121G>A MANE Select | NP_004351.1:p.Val41Met | |
| NM_001317184.2:c.121G>A | NP_001304113.1:p.Val41Met | |
| NM_001317185.2:c.-1495G>A | NP_001304114.1:n.-1495G>A | |
| NM_001317186.2:c.-1699G>A | NP_001304115.1:n.-1699G>A |