Linked Data
ClinVar Variation Id:
225415
dbSNP Id:
rs200662973
ExAC:
17:10436629 A / G
gnomAD v2:
17-10436629-A-G
gnomAD v3:
17-10533312-A-G
gnomAD v4:
17-10533312-A-G
COSMIC:
COSM2925369
PubMed:
PMID:22349865
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10533312A>G , CM000679.2:g.10533312A>G | GRCh38 |
| NC_000017.10:g.10436629A>G , CM000679.1:g.10436629A>G | GRCh37 |
| NC_000017.9:g.10377354A>G | NCBI36 |
| NG_013014.1:g.21389T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245503.10:c.2414T>C (MYH2) MANE Select | ENSP00000245503.5:p.Val805Ala | |
| ENST00000245503.9:c.2414T>C (MYH2) | ENSP00000245503.5:p.Val805Ala | |
| ENST00000397183.6:c.2414T>C (MYH2) | ENSP00000380367.2:p.Val805Ala | |
| ENST00000532183.6:c.1974+3218T>C (MYH2) | ENSP00000433944.1:n.1974+3218T>C | |
| ENST00000622564.4:c.1974+3218T>C (MYH2) | ENSP00000482463.1:n.1974+3218T>C | |
| NM_001100112.1:c.2414T>C (MYH2) | NP_001093582.1:p.Val805Ala | |
| NM_017534.5:c.2414T>C (MYH2) | NP_060004.3:p.Val805Ala | |
| NR_125367.1:n.168-34225A>G (MYHAS) | ||
| NM_017534.6:c.2414T>C (MYH2) MANE Select | NP_060004.3:p.Val805Ala | |
| NM_001100112.2:c.2414T>C (MYH2) | NP_001093582.1:p.Val805Ala |