Canonical Allele Identifier: CA2123450992
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431209C= , CM000676.2:g.23431209C= GRCh38
NC_000014.8:g.23900418C= , CM000676.1:g.23900418C= GRCh37
NC_000014.7:g.22970258C= NCBI36
NG_007884.1:g.9453G= , LRG_384:g.9453G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-210G= MANE Select ENSP00000347507.3:n.797-210G=
ENST00000355349.3:c.797-210G= ENSP00000347507.3:n.797-210G=
NM_000257.3:c.797-210G= NP_000248.2:n.797-210G=
XR_245686.3:n.903-210G=
XM_017021340.1:c.797-210G= XP_016876829.1:n.797-210G=
NM_000257.4:c.797-210G= MANE Select NP_000248.2:n.797-210G=