Canonical Allele Identifier: CA2580088028
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195946
ClinVar RCV Id: RCV002633287

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431749C>A , CM000676.2:g.23431749C>A GRCh38
NC_000014.8:g.23900958C>A , CM000676.1:g.23900958C>A GRCh37
NC_000014.7:g.22970798C>A NCBI36
NG_007884.1:g.8913G>T , LRG_384:g.8913G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.639+12G>T MANE Select ENSP00000347507.3:n.639+12G>T
ENST00000355349.3:c.639+12G>T ENSP00000347507.3:n.639+12G>T
NM_000257.3:c.639+12G>T NP_000248.2:n.639+12G>T
XR_245686.3:n.745+12G>T
XM_017021340.1:c.639+12G>T XP_016876829.1:n.639+12G>T
NM_000257.4:c.639+12G>T MANE Select NP_000248.2:n.639+12G>T