Canonical Allele Identifier: CA2123451358
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422534T= , CM000676.2:g.23422534T= GRCh38
NC_000014.8:g.23891743T= , CM000676.1:g.23891743T= GRCh37
NC_000014.7:g.22961583T= NCBI36
NG_007884.1:g.18128A= , LRG_384:g.18128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-209A= MANE Select ENSP00000347507.3:n.3100-209A=
ENST00000355349.3:c.3100-209A= ENSP00000347507.3:n.3100-209A=
NM_000257.3:c.3100-209A= NP_000248.2:n.3100-209A=
XR_245686.3:n.3206-209A=
XM_017021340.1:c.3100-209A= XP_016876829.1:n.3100-209A=
NM_000257.4:c.3100-209A= MANE Select NP_000248.2:n.3100-209A=