Canonical Allele Identifier: CA2123450880
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422288A= , CM000676.2:g.23422288A= GRCh38
NC_000014.8:g.23891497A= , CM000676.1:g.23891497A= GRCh37
NC_000014.7:g.22961337A= NCBI36
NG_007884.1:g.18374T= , LRG_384:g.18374T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.3137T= MANE Select ENSP00000347507.3:p.Met1046=
ENST00000355349.3:c.3137T= ENSP00000347507.3:p.Met1046=
NM_000257.3:c.3137T= NP_000248.2:p.Met1046=
XR_245686.3:n.3243T=
XM_017021340.1:c.3137T= XP_016876829.1:p.Met1046=
NM_000257.4:c.3137T= MANE Select NP_000248.2:p.Met1046=