Canonical Allele Identifier: CA2123452771
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431831C= , CM000676.2:g.23431831C= GRCh38
NC_000014.8:g.23901040C= , CM000676.1:g.23901040C= GRCh37
NC_000014.7:g.22970880C= NCBI36
NG_007884.1:g.8831G= , LRG_384:g.8831G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.569G= MANE Select ENSP00000347507.3:p.Arg190=
ENST00000355349.3:c.569G= ENSP00000347507.3:p.Arg190=
NM_000257.3:c.569G= NP_000248.2:p.Arg190=
XR_245686.3:n.675G=
XM_017021340.1:c.569G= XP_016876829.1:p.Arg190=
NM_000257.4:c.569G= MANE Select NP_000248.2:p.Arg190=