Linked Data
ClinVar Variation Id:
134717
dbSNP Id:
rs73302195
ExAC:
12:49426878 C / T
gnomAD v2:
12-49426878-C-T
gnomAD v3:
12-49033095-C-T
gnomAD v4:
12-49033095-C-T
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49033095C>T , CM000674.2:g.49033095C>T | GRCh38 |
| NC_000012.11:g.49426878C>T , CM000674.1:g.49426878C>T | GRCh37 |
| NC_000012.10:g.47713145C>T | NCBI36 |
| NG_027827.1:g.27230G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.11610G>A | ENSP00000506726.1:p.Met3870Ile | |
| ENST00000685166.1:c.11619G>A | ENSP00000509386.1:p.Met3873Ile | |
| ENST00000685554.1:c.1170G>A | ENSP00000508640.1:p.Met390Ile | |
| ENST00000687201.1:c.3189G>A | ENSP00000510037.1:p.Met1063Ile | |
| ENST00000692637.1:c.11607G>A | ENSP00000509666.1:p.Met3869Ile | |
| ENST00000692841.1:c.3089G>A | ENSP00000508711.1:n.3089G>A | |
| ENST00000301067.12:c.11610G>A MANE Select | ENSP00000301067.7:p.Met3870Ile | |
| ENST00000301067.11:c.11610G>A | ENSP00000301067.7:p.Met3870Ile | |
| NM_003482.3:c.11610G>A | NP_003473.3:p.Met3870Ile | |
| XM_005269162.3:c.11610G>A | XP_005269219.1:p.Met3870Ile | |
| XM_006719614.2:c.11619G>A | XP_006719677.1:p.Met3873Ile | |
| XM_006719616.2:c.11607G>A | XP_006719679.1:p.Met3869Ile | |
| XM_011538770.1:c.11619G>A | XP_011537072.1:p.Met3873Ile | |
| XM_011538771.1:c.11616G>A | XP_011537073.1:p.Met3872Ile | |
| XM_011538772.1:c.11610G>A | XP_011537074.1:p.Met3870Ile | |
| XM_011538773.1:c.11607G>A | XP_011537075.1:p.Met3869Ile | |
| XM_011538774.1:c.11598G>A | XP_011537076.1:p.Met3866Ile | |
| XM_011538775.1:c.11619G>A | XP_011537077.1:p.Met3873Ile | |
| XM_011538776.1:c.11526G>A | XP_011537078.1:p.Met3842Ile | |
| XR_944740.1:n.13939G>A | ||
| XM_005269162.4:c.11610G>A | XP_005269219.1:p.Met3870Ile | |
| XM_006719614.4:c.11619G>A | XP_006719677.1:p.Met3873Ile | |
| XM_006719616.3:c.11607G>A | XP_006719679.1:p.Met3869Ile | |
| XM_011538770.2:c.11619G>A | XP_011537072.1:p.Met3873Ile | |
| XM_011538771.2:c.11616G>A | XP_011537073.1:p.Met3872Ile | |
| XM_011538772.2:c.11610G>A | XP_011537074.1:p.Met3870Ile | |
| XM_011538773.2:c.11607G>A | XP_011537075.1:p.Met3869Ile | |
| XM_011538774.2:c.11598G>A | XP_011537076.1:p.Met3866Ile | |
| XM_011538776.2:c.11526G>A | XP_011537078.1:p.Met3842Ile | |
| XR_001748874.1:n.12928G>A | ||
| NM_003482.4:c.11610G>A MANE Select | NP_003473.3:p.Met3870Ile |