Canonical Allele Identifier: CA2123458232
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413814A= , CM000676.2:g.23413814A= GRCh38
NC_000014.8:g.23883023A= , CM000676.1:g.23883023A= GRCh37
NC_000014.7:g.22952863A= NCBI36
NG_007884.1:g.26848T= , LRG_384:g.26848T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5735T= MANE Select ENSP00000347507.3:p.Ile1912=
ENST00000355349.3:c.5735T= ENSP00000347507.3:p.Ile1912=
NM_000257.3:c.5735T= NP_000248.2:p.Ile1912=
XM_017021340.1:c.5735T= XP_016876829.1:p.Ile1912=
NM_000257.4:c.5735T= MANE Select NP_000248.2:p.Ile1912=