Canonical Allele Identifier: CA2123450158
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421992C= , CM000676.2:g.23421992C= GRCh38
NC_000014.8:g.23891201C= , CM000676.1:g.23891201C= GRCh37
NC_000014.7:g.22961041C= NCBI36
NG_007884.1:g.18670G= , LRG_384:g.18670G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+188G= MANE Select ENSP00000347507.3:n.3245+188G=
ENST00000355349.3:c.3245+188G= ENSP00000347507.3:n.3245+188G=
NM_000257.3:c.3245+188G= NP_000248.2:n.3245+188G=
XR_245686.3:n.3351+188G=
XM_017021340.1:c.3245+188G= XP_016876829.1:n.3245+188G=
NM_000257.4:c.3245+188G= MANE Select NP_000248.2:n.3245+188G=