Canonical Allele Identifier: CA2123453471
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423710G= , CM000676.2:g.23423710G= GRCh38
NC_000014.8:g.23892919G= , CM000676.1:g.23892919G= GRCh37
NC_000014.7:g.22962759G= NCBI36
NG_007884.1:g.16952C= , LRG_384:g.16952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2936C= MANE Select ENSP00000347507.3:p.Thr979=
ENST00000355349.3:c.2936C= ENSP00000347507.3:p.Thr979=
NM_000257.3:c.2936C= NP_000248.2:p.Thr979=
XR_245686.3:n.3042C=
XM_017021340.1:c.2936C= XP_016876829.1:p.Thr979=
NM_000257.4:c.2936C= MANE Select NP_000248.2:p.Thr979=