Canonical Allele Identifier: CA2123453879
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423921C= , CM000676.2:g.23423921C= GRCh38
NC_000014.8:g.23893130C= , CM000676.1:g.23893130C= GRCh37
NC_000014.7:g.22962970C= NCBI36
NG_007884.1:g.16741G= , LRG_384:g.16741G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2908G= MANE Select ENSP00000347507.3:p.Ala970=
ENST00000355349.3:c.2908G= ENSP00000347507.3:p.Ala970=
NM_000257.3:c.2908G= NP_000248.2:p.Ala970=
XR_245686.3:n.3014G=
XM_017021340.1:c.2908G= XP_016876829.1:p.Ala970=
NM_000257.4:c.2908G= MANE Select NP_000248.2:p.Ala970=