Canonical Allele Identifier: CA2123448304
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420818A= , CM000676.2:g.23420818A= GRCh38
NC_000014.8:g.23890027A= , CM000676.1:g.23890027A= GRCh37
NC_000014.7:g.22959867A= NCBI36
NG_007884.1:g.19844T= , LRG_384:g.19844T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+140T= MANE Select ENSP00000347507.3:n.3336+140T=
ENST00000355349.3:c.3336+140T= ENSP00000347507.3:n.3336+140T=
NM_000257.3:c.3336+140T= NP_000248.2:n.3336+140T=
XR_245686.3:n.3444+140T=
XM_017021340.1:c.3336+140T= XP_016876829.1:n.3336+140T=
NM_000257.4:c.3336+140T= MANE Select NP_000248.2:n.3336+140T=