Linked Data
dbSNP Id:
rs2120410982
gnomAD v4:
12-49030911-C-T
MyVariant Identifiers:
chr12:g.49424694C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49030911C>T , CM000674.2:g.49030911C>T | GRCh38 |
| NC_000012.11:g.49424694C>T , CM000674.1:g.49424694C>T | GRCh37 |
| NC_000012.10:g.47710961C>T | NCBI36 |
| NG_027827.1:g.29414G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000552391.2:n.353G>A | ||
| ENST00000683543.2:c.13653G>A | ENSP00000506726.1:p.Leu4551= | |
| ENST00000685166.1:c.13662G>A | ENSP00000509386.1:p.Leu4554= | |
| ENST00000685982.1:c.139-143G>A | ENSP00000508613.1:n.139-143G>A | |
| ENST00000691986.1:c.138+264G>A | ENSP00000509196.1:n.138+264G>A | |
| ENST00000692637.1:c.13650G>A | ENSP00000509666.1:p.Leu4550= | |
| ENST00000692973.1:c.254G>A | ENSP00000508893.1:n.254G>A | |
| ENST00000301067.12:c.13653G>A MANE Select | ENSP00000301067.7:p.Leu4551= | |
| ENST00000301067.11:c.13653G>A | ENSP00000301067.7:p.Leu4551= | |
| ENST00000552391.1:n.353G>A | ||
| NM_003482.3:c.13653G>A | NP_003473.3:p.Leu4551= | |
| XM_005269162.3:c.13653G>A | XP_005269219.1:p.Leu4551= | |
| XM_006719614.2:c.13662G>A | XP_006719677.1:p.Leu4554= | |
| XM_006719616.2:c.13650G>A | XP_006719679.1:p.Leu4550= | |
| XM_011538770.1:c.13662G>A | XP_011537072.1:p.Leu4554= | |
| XM_011538771.1:c.13659G>A | XP_011537073.1:p.Leu4553= | |
| XM_011538772.1:c.13653G>A | XP_011537074.1:p.Leu4551= | |
| XM_011538773.1:c.13650G>A | XP_011537075.1:p.Leu4550= | |
| XM_011538774.1:c.13641G>A | XP_011537076.1:p.Leu4547= | |
| XM_011538775.1:c.13662G>A | XP_011537077.1:p.Leu4554= | |
| XM_011538776.1:c.13569G>A | XP_011537078.1:p.Leu4523= | |
| XR_944740.1:n.15982G>A | ||
| XM_005269162.4:c.13653G>A | XP_005269219.1:p.Leu4551= | |
| XM_006719614.4:c.13662G>A | XP_006719677.1:p.Leu4554= | |
| XM_006719616.3:c.13650G>A | XP_006719679.1:p.Leu4550= | |
| XM_011538770.2:c.13662G>A | XP_011537072.1:p.Leu4554= | |
| XM_011538771.2:c.13659G>A | XP_011537073.1:p.Leu4553= | |
| XM_011538772.2:c.13653G>A | XP_011537074.1:p.Leu4551= | |
| XM_011538773.2:c.13650G>A | XP_011537075.1:p.Leu4550= | |
| XM_011538774.2:c.13641G>A | XP_011537076.1:p.Leu4547= | |
| XM_011538776.2:c.13569G>A | XP_011537078.1:p.Leu4523= | |
| XR_001748874.1:n.14971G>A | ||
| NM_003482.4:c.13653G>A MANE Select | NP_003473.3:p.Leu4551= |