Canonical Allele Identifier: CA2123453910
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423930C= , CM000676.2:g.23423930C= GRCh38
NC_000014.8:g.23893139C= , CM000676.1:g.23893139C= GRCh37
NC_000014.7:g.22962979C= NCBI36
NG_007884.1:g.16732G= , LRG_384:g.16732G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2899G= MANE Select ENSP00000347507.3:p.Glu967=
ENST00000355349.3:c.2899G= ENSP00000347507.3:p.Glu967=
NM_000257.3:c.2899G= NP_000248.2:p.Glu967=
XR_245686.3:n.3005G=
XM_017021340.1:c.2899G= XP_016876829.1:p.Glu967=
NM_000257.4:c.2899G= MANE Select NP_000248.2:p.Glu967=