Canonical Allele Identifier: CA2123455684
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1893032398

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433532del , CM000676.2:g.23433532del GRCh38
NC_000014.8:g.23902741del , CM000676.1:g.23902741del GRCh37
NC_000014.7:g.22972581del NCBI36
NG_007884.1:g.7131del , LRG_384:g.7131del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.201+1del
ENST00000355349.3:c.201+1del
NM_000257.3:c.201+1del
XR_245686.3:n.307+1del
XM_017021340.1:c.201+1del
NM_000257.4:c.201+1del