Linked Data
ClinVar Variation Id:
1244297
ClinVar RCV Id:
RCV001648562
dbSNP Id:
rs2138642700
MyVariant Identifiers:
chr14:g.23885515G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23416306G>A , CM000676.2:g.23416306G>A | GRCh38 |
| NC_000014.8:g.23885515G>A , CM000676.1:g.23885515G>A | GRCh37 |
| NC_000014.7:g.22955355G>A | NCBI36 |
| NG_007884.1:g.24356C>T , LRG_384:g.24356C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.4651C>T (MYH7) MANE Select | ENSP00000347507.3:p.Leu1551= | |
| ENST00000355349.3:c.4651C>T (MYH7) | ENSP00000347507.3:p.Leu1551= | |
| NM_000257.3:c.4651C>T (MYH7) | NP_000248.2:p.Leu1551= | |
| NR_126491.1:n.558+9G>A (MHRT) | ||
| XM_017021340.1:c.4651C>T (MYH7) | XP_016876829.1:p.Leu1551= | |
| NM_000257.4:c.4651C>T (MYH7) MANE Select | NP_000248.2:p.Leu1551= |