Linked Data
ClinVar Variation Id:
1594669
ClinVar RCV Id:
RCV002107998
dbSNP Id:
rs1595073441
MyVariant Identifiers:
chr14:g.23885357T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23416148T>C , CM000676.2:g.23416148T>C | GRCh38 |
| NC_000014.8:g.23885357T>C , CM000676.1:g.23885357T>C | GRCh37 |
| NC_000014.7:g.22955197T>C | NCBI36 |
| NG_007884.1:g.24514A>G , LRG_384:g.24514A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.4809A>G (MYH7) MANE Select | ENSP00000347507.3:p.Ala1603= | |
| ENST00000355349.3:c.4809A>G (MYH7) | ENSP00000347507.3:p.Ala1603= | |
| NM_000257.3:c.4809A>G (MYH7) | NP_000248.2:p.Ala1603= | |
| NR_126491.1:n.409T>C (MHRT) | ||
| XM_017021340.1:c.4809A>G (MYH7) | XP_016876829.1:p.Ala1603= | |
| NM_000257.4:c.4809A>G (MYH7) MANE Select | NP_000248.2:p.Ala1603= |