Canonical Allele Identifier: CA2123453468
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423709T= , CM000676.2:g.23423709T= GRCh38
NC_000014.8:g.23892918T= , CM000676.1:g.23892918T= GRCh37
NC_000014.7:g.22962758T= NCBI36
NG_007884.1:g.16953A= , LRG_384:g.16953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2937A= MANE Select ENSP00000347507.3:p.Thr979=
ENST00000355349.3:c.2937A= ENSP00000347507.3:p.Thr979=
NM_000257.3:c.2937A= NP_000248.2:p.Thr979=
XR_245686.3:n.3043A=
XM_017021340.1:c.2937A= XP_016876829.1:p.Thr979=
NM_000257.4:c.2937A= MANE Select NP_000248.2:p.Thr979=