Canonical Allele Identifier: CA2123455962
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433665C= , CM000676.2:g.23433665C= GRCh38
NC_000014.8:g.23902874C= , CM000676.1:g.23902874C= GRCh37
NC_000014.7:g.22972714C= NCBI36
NG_007884.1:g.6997G= , LRG_384:g.6997G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.68G= MANE Select ENSP00000347507.3:p.Arg23=
ENST00000355349.3:c.68G= ENSP00000347507.3:p.Arg23=
NM_000257.3:c.68G= NP_000248.2:p.Arg23=
XR_245686.3:n.174G=
XM_017021340.1:c.68G= XP_016876829.1:p.Arg23=
NM_000257.4:c.68G= MANE Select NP_000248.2:p.Arg23=