Canonical Allele Identifier: CA2123455027
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424337G= , CM000676.2:g.23424337G= GRCh38
NC_000014.8:g.23893546G= , CM000676.1:g.23893546G= GRCh37
NC_000014.7:g.22963386G= NCBI36
NG_007884.1:g.16325C= , LRG_384:g.16325C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-188C= MANE Select ENSP00000347507.3:n.2680-188C=
ENST00000355349.3:c.2680-188C= ENSP00000347507.3:n.2680-188C=
NM_000257.3:c.2680-188C= NP_000248.2:n.2680-188C=
XR_245686.3:n.2786-188C=
XM_017021340.1:c.2680-188C= XP_016876829.1:n.2680-188C=
NM_000257.4:c.2680-188C= MANE Select NP_000248.2:n.2680-188C=