Linked Data
ClinVar Variation Id:
2917704
ClinVar RCV Id:
RCV003749741
dbSNP Id:
rs1892193216
gnomAD v4:
14-23416091-G-A
MyVariant Identifiers:
chr14:g.23885300G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23416091G>A , CM000676.2:g.23416091G>A | GRCh38 |
| NC_000014.8:g.23885300G>A , CM000676.1:g.23885300G>A | GRCh37 |
| NC_000014.7:g.22955140G>A | NCBI36 |
| NG_007884.1:g.24571C>T , LRG_384:g.24571C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.4866C>T (MYH7) MANE Select | ENSP00000347507.3:p.Leu1622= | |
| ENST00000355349.3:c.4866C>T (MYH7) | ENSP00000347507.3:p.Leu1622= | |
| NM_000257.3:c.4866C>T (MYH7) | NP_000248.2:p.Leu1622= | |
| NR_126491.1:n.352G>A (MHRT) | ||
| XM_017021340.1:c.4866C>T (MYH7) | XP_016876829.1:p.Leu1622= | |
| NM_000257.4:c.4866C>T (MYH7) MANE Select | NP_000248.2:p.Leu1622= |