Canonical Allele Identifier: CA2123462590
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415238C= , CM000676.2:g.23415238C= GRCh38
NC_000014.8:g.23884447C= , CM000676.1:g.23884447C= GRCh37
NC_000014.7:g.22954287C= NCBI36
NG_007884.1:g.25424G= , LRG_384:g.25424G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5316G= MANE Select ENSP00000347507.3:p.Glu1772=
ENST00000355349.3:c.5316G= ENSP00000347507.3:p.Glu1772=
NM_000257.3:c.5316G= NP_000248.2:p.Glu1772=
XM_017021340.1:c.5316G= XP_016876829.1:p.Glu1772=
NM_000257.4:c.5316G= MANE Select NP_000248.2:p.Glu1772=