Canonical Allele Identifier: CA2123455153
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424412G= , CM000676.2:g.23424412G= GRCh38
NC_000014.8:g.23893621G= , CM000676.1:g.23893621G= GRCh37
NC_000014.7:g.22963461G= NCBI36
NG_007884.1:g.16250C= , LRG_384:g.16250C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-263C= MANE Select ENSP00000347507.3:n.2680-263C=
ENST00000355349.3:c.2680-263C= ENSP00000347507.3:n.2680-263C=
NM_000257.3:c.2680-263C= NP_000248.2:n.2680-263C=
XR_245686.3:n.2786-263C=
XM_017021340.1:c.2680-263C= XP_016876829.1:n.2680-263C=
NM_000257.4:c.2680-263C= MANE Select NP_000248.2:n.2680-263C=