Canonical Allele Identifier: CA2123455746
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433558C= , CM000676.2:g.23433558C= GRCh38
NC_000014.8:g.23902767C= , CM000676.1:g.23902767C= GRCh37
NC_000014.7:g.22972607C= NCBI36
NG_007884.1:g.7104G= , LRG_384:g.7104G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.175G= MANE Select ENSP00000347507.3:p.Val59=
ENST00000355349.3:c.175G= ENSP00000347507.3:p.Val59=
NM_000257.3:c.175G= NP_000248.2:p.Val59=
XR_245686.3:n.281G=
XM_017021340.1:c.175G= XP_016876829.1:p.Val59=
NM_000257.4:c.175G= MANE Select NP_000248.2:p.Val59=