Linked Data
ClinVar Variation Id:
1360530
ClinVar RCV Id:
RCV001904934
dbSNP Id:
rs2141137587
gnomAD v4:
16-9764816-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9764816T>C , CM000678.2:g.9764816T>C | GRCh38 |
| NC_000016.9:g.9858673T>C , CM000678.1:g.9858673T>C | GRCh37 |
| NC_000016.8:g.9766174T>C | NCBI36 |
| NG_011812.1:g.422939A>G | |
| NG_011812.2:g.422939A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330684.4:c.2728A>G MANE Select | ENSP00000332549.3:p.Met910Val | |
| ENST00000535259.6:c.2257A>G | ENSP00000441572.3:p.Met753Val | |
| ENST00000636273.2:n.2321A>G | ||
| ENST00000674742.1:c.2257A>G | ENSP00000502200.1:p.Met753Val | |
| ENST00000675398.1:c.*98A>G | ENSP00000502752.1:n.*98A>G | |
| ENST00000330684.3:c.2728A>G | ENSP00000332549.3:p.Met910Val | |
| ENST00000396573.6:c.2728A>G | ENSP00000379818.2:p.Met910Val | |
| ENST00000396575.6:c.2317A>G | ENSP00000379820.3:p.Met773Val | |
| ENST00000461292.3:n.2367A>G | ||
| ENST00000535259.5:c.2317A>G | ENSP00000441572.2:p.Met773Val | |
| ENST00000562109.5:c.2728A>G | ENSP00000454998.1:p.Met910Val | |
| NM_000833.4:c.2728A>G | NP_000824.1:p.Met910Val | |
| NM_001134407.2:c.2728A>G | NP_001127879.1:p.Met910Val | |
| NM_001134408.2:c.2728A>G | NP_001127880.1:p.Met910Val | |
| XM_011522456.1:c.2569A>G | XP_011520758.1:p.Met857Val | |
| XM_011522457.1:c.2470A>G | XP_011520759.1:p.Met824Val | |
| XM_011522458.1:c.2257A>G | XP_011520760.1:p.Met753Val | |
| XM_011522459.1:c.2257A>G | XP_011520761.1:p.Met753Val | |
| XM_011522460.1:c.2257A>G | XP_011520762.1:p.Met753Val | |
| XM_011522461.1:c.2728A>G | XP_011520763.1:p.Met910Val | |
| XM_011522458.3:c.2257A>G | XP_011520760.1:p.Met753Val | |
| XM_011522461.3:c.2728A>G | XP_011520763.1:p.Met910Val | |
| XM_017023172.1:c.2884A>G | XP_016878661.1:p.Met962Val | |
| XM_017023173.1:c.2884A>G | XP_016878662.1:p.Met962Val | |
| NM_001134407.3:c.2728A>G MANE Select | NP_001127879.1:p.Met910Val | |
| NM_000833.5:c.2728A>G | NP_000824.1:p.Met910Val |