Canonical Allele Identifier: CA2123448196
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420751C= , CM000676.2:g.23420751C= GRCh38
NC_000014.8:g.23889960C= , CM000676.1:g.23889960C= GRCh37
NC_000014.7:g.22959800C= NCBI36
NG_007884.1:g.19911G= , LRG_384:g.19911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+207G= MANE Select ENSP00000347507.3:n.3336+207G=
ENST00000355349.3:c.3336+207G= ENSP00000347507.3:n.3336+207G=
NM_000257.3:c.3336+207G= NP_000248.2:n.3336+207G=
XR_245686.3:n.3444+207G=
XM_017021340.1:c.3336+207G= XP_016876829.1:n.3336+207G=
NM_000257.4:c.3336+207G= MANE Select NP_000248.2:n.3336+207G=