Canonical Allele Identifier: CA2123462585
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415237G= , CM000676.2:g.23415237G= GRCh38
NC_000014.8:g.23884446G= , CM000676.1:g.23884446G= GRCh37
NC_000014.7:g.22954286G= NCBI36
NG_007884.1:g.25425C= , LRG_384:g.25425C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5317C= MANE Select ENSP00000347507.3:p.Gln1773=
ENST00000355349.3:c.5317C= ENSP00000347507.3:p.Gln1773=
NM_000257.3:c.5317C= NP_000248.2:p.Gln1773=
XM_017021340.1:c.5317C= XP_016876829.1:p.Gln1773=
NM_000257.4:c.5317C= MANE Select NP_000248.2:p.Gln1773=