Canonical Allele Identifier: CA2123462348
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415180C= , CM000676.2:g.23415180C= GRCh38
NC_000014.8:g.23884389C= , CM000676.1:g.23884389C= GRCh37
NC_000014.7:g.22954229C= NCBI36
NG_007884.1:g.25482G= , LRG_384:g.25482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5374G= MANE Select ENSP00000347507.3:p.Asp1792=
ENST00000355349.3:c.5374G= ENSP00000347507.3:p.Asp1792=
NM_000257.3:c.5374G= NP_000248.2:p.Asp1792=
XM_017021340.1:c.5374G= XP_016876829.1:p.Asp1792=
NM_000257.4:c.5374G= MANE Select NP_000248.2:p.Asp1792=