Canonical Allele Identifier: CA2123452946
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423516A= , CM000676.2:g.23423516A= GRCh38
NC_000014.8:g.23892725A= , CM000676.1:g.23892725A= GRCh37
NC_000014.7:g.22962565A= NCBI36
NG_007884.1:g.17146T= , LRG_384:g.17146T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+31T= MANE Select ENSP00000347507.3:n.3099+31T=
ENST00000355349.3:c.3099+31T= ENSP00000347507.3:n.3099+31T=
NM_000257.3:c.3099+31T= NP_000248.2:n.3099+31T=
XR_245686.3:n.3205+31T=
XM_017021340.1:c.3099+31T= XP_016876829.1:n.3099+31T=
NM_000257.4:c.3099+31T= MANE Select NP_000248.2:n.3099+31T=