Canonical Allele Identifier: CA2123444959
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419436T= , CM000676.2:g.23419436T= GRCh38
NC_000014.8:g.23888645T= , CM000676.1:g.23888645T= GRCh37
NC_000014.7:g.22958485T= NCBI36
NG_007884.1:g.21226A= , LRG_384:g.21226A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3853+47A= MANE Select ENSP00000347507.3:n.3853+47A=
ENST00000355349.3:c.3853+47A= ENSP00000347507.3:n.3853+47A=
NM_000257.3:c.3853+47A= NP_000248.2:n.3853+47A=
XM_017021340.1:c.3853+47A= XP_016876829.1:n.3853+47A=
NM_000257.4:c.3853+47A= MANE Select NP_000248.2:n.3853+47A=