Linked Data
ClinVar Variation Id:
136295
dbSNP Id:
rs35582308
ExAC:
1:227149153 G / A
gnomAD v2:
1-227149153-G-A
gnomAD v3:
1-226961452-G-A
gnomAD v4:
1-226961452-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.226961452G>A , CM000663.2:g.226961452G>A | GRCh38 |
| NC_000001.10:g.227149153G>A , CM000663.1:g.227149153G>A | GRCh37 |
| NC_000001.9:g.225215776G>A | NCBI36 |
| NG_012825.1:g.26216G>A | |
| NG_012825.2:g.68917G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366777.4:c.67G>A MANE Select | ENSP00000355739.3:p.Val23Met | |
| ENST00000366779.6:c.*4794G>A | ENSP00000355741.2:n.*4794G>A | |
| ENST00000676884.1:c.*4916G>A | ENSP00000503200.1:n.*4916G>A | |
| ENST00000366777.3:c.67G>A | ENSP00000355739.3:p.Val23Met | |
| ENST00000366778.5:c.-34-56G>A | ENSP00000355740.1:n.-34-56G>A | |
| ENST00000366779.5:c.67G>A | ENSP00000355741.1:p.Val23Met | |
| ENST00000478406.5:n.107-15997G>A | ||
| ENST00000489044.1:n.278G>A | ||
| NM_020247.4:c.67G>A | NP_064632.2:p.Val23Met | |
| XM_005273201.1:c.67G>A | XP_005273258.1:p.Val23Met | |
| XM_011544238.1:c.67G>A | XP_011542540.1:p.Val23Met | |
| XM_011544239.1:c.67G>A | XP_011542541.1:p.Val23Met | |
| XM_011544240.1:c.67G>A | XP_011542542.1:p.Val23Met | |
| XM_011544241.1:c.67G>A | XP_011542543.1:p.Val23Met | |
| XM_011544239.2:c.67G>A | XP_011542541.1:p.Val23Met | |
| XM_011544241.2:c.67G>A | XP_011542543.1:p.Val23Met | |
| XM_017001852.1:c.67G>A | XP_016857341.1:p.Val23Met | |
| XM_024448517.1:c.67G>A | XP_024304285.1:p.Val23Met | |
| XM_024448518.1:c.67G>A | XP_024304286.1:p.Val23Met | |
| NM_020247.5:c.67G>A MANE Select | NP_064632.2:p.Val23Met |