Canonical Allele Identifier: CA2123458522
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413860G= , CM000676.2:g.23413860G= GRCh38
NC_000014.8:g.23883069G= , CM000676.1:g.23883069G= GRCh37
NC_000014.7:g.22952909G= NCBI36
NG_007884.1:g.26802C= , LRG_384:g.26802C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5689C= MANE Select ENSP00000347507.3:p.Arg1897=
ENST00000355349.3:c.5689C= ENSP00000347507.3:p.Arg1897=
NM_000257.3:c.5689C= NP_000248.2:p.Arg1897=
XM_017021340.1:c.5689C= XP_016876829.1:p.Arg1897=
NM_000257.4:c.5689C= MANE Select NP_000248.2:p.Arg1897=