Linked Data
ClinVar Variation Id:
167038
dbSNP Id:
rs150452237
ExAC:
6:146007358 T / C
gnomAD v2:
6-146007358-T-C
gnomAD v3:
6-145686222-T-C
gnomAD v4:
6-145686222-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.145686222T>C , CM000668.2:g.145686222T>C | GRCh38 |
| NC_000006.11:g.146007358T>C , CM000668.1:g.146007358T>C | GRCh37 |
| NC_000006.10:g.146049051T>C | NCBI36 |
| NG_012832.1:g.54634A>G | |
| NG_012832.2:g.54634A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367519.9:c.376A>G MANE Select | ENSP00000356489.3:p.Ile126Val | |
| ENST00000435470.2:c.376A>G | ENSP00000405913.2:p.Ile126Val | |
| ENST00000496228.2:n.183A>G | ||
| ENST00000611340.5:c.-39A>G | ENSP00000480268.1:n.-39A>G | |
| ENST00000638262.1:c.376A>G | ENSP00000492876.1:p.Ile126Val | |
| ENST00000638554.1:c.154A>G | ENSP00000492823.1:p.Ile52Val | |
| ENST00000638717.1:c.159A>G | ||
| ENST00000638778.1:c.-39A>G | ENSP00000491353.1:n.-39A>G | |
| ENST00000638783.1:c.-39A>G | ENSP00000491338.1:n.-39A>G | |
| ENST00000639049.1:c.603A>G | ||
| ENST00000639423.1:c.-39A>G | ENSP00000492701.1:n.-39A>G | |
| ENST00000639465.1:c.-39A>G | ENSP00000491180.1:n.-39A>G | |
| ENST00000639799.1:n.917A>G | ||
| ENST00000639849.1:c.-39A>G | ENSP00000491224.1:n.-39A>G | |
| ENST00000640225.1:c.-39A>G | ENSP00000492179.1:n.-39A>G | |
| ENST00000640297.1:n.317+48976A>G | ||
| ENST00000640351.1:c.112A>G | ||
| ENST00000640426.2:n.88A>G | ||
| ENST00000640898.1:n.157A>G | ||
| ENST00000640980.1:c.-39A>G | ENSP00000491191.1:n.-39A>G | |
| ENST00000367519.7:c.376A>G | ENSP00000356489.3:p.Ile126Val | |
| ENST00000435470.1:c.135A>G | ||
| ENST00000450221.5:c.75A>G | ||
| ENST00000461700.1:n.136+18A>G | ||
| ENST00000496228.1:n.109A>G | ||
| ENST00000611340.4:c.-39A>G | ENSP00000480268.1:n.-39A>G | |
| ENST00000618445.4:c.376A>G | ENSP00000480339.1:p.Ile126Val | |
| NM_001018041.1:c.376A>G | NP_001018051.1:p.Ile126Val | |
| NM_005670.3:c.376A>G | NP_005661.1:p.Ile126Val | |
| XM_006715564.2:c.376A>G | XP_006715627.1:p.Ile126Val | |
| XM_011536113.1:c.376A>G | XP_011534415.1:p.Ile126Val | |
| XM_011536114.1:c.376A>G | XP_011534416.1:p.Ile126Val | |
| XM_011536115.1:c.376A>G | XP_011534417.1:p.Ile126Val | |
| XM_011536116.1:c.-39A>G | XP_011534418.1:n.-39A>G | |
| NM_001360057.1:c.376A>G | NP_001346986.1:p.Ile126Val | |
| NM_001360064.1:c.-39A>G | NP_001346993.1:n.-39A>G | |
| NM_001360071.1:c.-39A>G | NP_001347000.1:n.-39A>G | |
| NR_153397.1:n.398A>G | ||
| NR_153398.1:n.189A>G | ||
| XM_011536113.2:c.376A>G | XP_011534415.1:p.Ile126Val | |
| XM_024446550.1:c.376A>G | XP_024302318.1:p.Ile126Val | |
| XM_024446551.1:c.-39A>G | XP_024302319.1:n.-39A>G | |
| NM_005670.4:c.376A>G MANE Select | NP_005661.1:p.Ile126Val | |
| NM_001018041.2:c.376A>G | NP_001018051.1:p.Ile126Val | |
| NM_001360057.2:c.376A>G | NP_001346986.1:p.Ile126Val | |
| NM_001360064.2:c.-39A>G | NP_001346993.1:n.-39A>G | |
| NM_001360071.2:c.-39A>G | NP_001347000.1:n.-39A>G | |
| NM_001368129.2:c.-248A>G | NP_001355058.1:n.-248A>G | |
| NM_001368130.1:c.376A>G | NP_001355059.1:p.Ile126Val | |
| NM_001368131.1:c.-39A>G | NP_001355060.1:n.-39A>G | |
| NM_001368132.1:c.-248A>G | NP_001355061.1:n.-248A>G | |
| NR_153398.2:n.191A>G |