Canonical Allele Identifier: CA2123450381
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422159A= , CM000676.2:g.23422159A= GRCh38
NC_000014.8:g.23891368A= , CM000676.1:g.23891368A= GRCh37
NC_000014.7:g.22961208A= NCBI36
NG_007884.1:g.18503T= , LRG_384:g.18503T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+21T= MANE Select ENSP00000347507.3:n.3245+21T=
ENST00000355349.3:c.3245+21T= ENSP00000347507.3:n.3245+21T=
NM_000257.3:c.3245+21T= NP_000248.2:n.3245+21T=
XR_245686.3:n.3351+21T=
XM_017021340.1:c.3245+21T= XP_016876829.1:n.3245+21T=
NM_000257.4:c.3245+21T= MANE Select NP_000248.2:n.3245+21T=