Linked Data
ClinVar Variation Id:
626537
ClinVar RCV Id:
RCV000769434
dbSNP Id:
rs1566522989
gnomAD v4:
14-23415474-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23415474C>G , CM000676.2:g.23415474C>G | GRCh38 |
| NC_000014.8:g.23884683C>G , CM000676.1:g.23884683C>G | GRCh37 |
| NC_000014.7:g.22954523C>G | NCBI36 |
| NG_007884.1:g.25188G>C , LRG_384:g.25188G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.5190G>C (MYH7) MANE Select | ENSP00000347507.3:p.Met1730Ile | |
| ENST00000355349.3:c.5190G>C (MYH7) | ENSP00000347507.3:p.Met1730Ile | |
| NM_000257.3:c.5190G>C (MYH7) | NP_000248.2:p.Met1730Ile | |
| NR_126491.1:n.25C>G (MHRT) | ||
| XM_017021340.1:c.5190G>C (MYH7) | XP_016876829.1:p.Met1730Ile | |
| NM_000257.4:c.5190G>C (MYH7) MANE Select | NP_000248.2:p.Met1730Ile |