Canonical Allele Identifier: CA2123455952
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433658T= , CM000676.2:g.23433658T= GRCh38
NC_000014.8:g.23902867T= , CM000676.1:g.23902867T= GRCh37
NC_000014.7:g.22972707T= NCBI36
NG_007884.1:g.7004A= , LRG_384:g.7004A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.75A= MANE Select ENSP00000347507.3:p.Glu25=
ENST00000355349.3:c.75A= ENSP00000347507.3:p.Glu25=
NM_000257.3:c.75A= NP_000248.2:p.Glu25=
XR_245686.3:n.181A=
XM_017021340.1:c.75A= XP_016876829.1:p.Glu25=
NM_000257.4:c.75A= MANE Select NP_000248.2:p.Glu25=