Canonical Allele Identifier: CA2123453850
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423911T= , CM000676.2:g.23423911T= GRCh38
NC_000014.8:g.23893120T= , CM000676.1:g.23893120T= GRCh37
NC_000014.7:g.22962960T= NCBI36
NG_007884.1:g.16751A= , LRG_384:g.16751A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2918A= MANE Select ENSP00000347507.3:p.Asn973=
ENST00000355349.3:c.2918A= ENSP00000347507.3:p.Asn973=
NM_000257.3:c.2918A= NP_000248.2:p.Asn973=
XR_245686.3:n.3024A=
XM_017021340.1:c.2918A= XP_016876829.1:p.Asn973=
NM_000257.4:c.2918A= MANE Select NP_000248.2:p.Asn973=