Canonical Allele Identifier: CA2123452156
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431622T= , CM000676.2:g.23431622T= GRCh38
NC_000014.8:g.23900831T= , CM000676.1:g.23900831T= GRCh37
NC_000014.7:g.22970671T= NCBI36
NG_007884.1:g.9040A= , LRG_384:g.9040A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.695A= MANE Select ENSP00000347507.3:p.Asn232=
ENST00000355349.3:c.695A= ENSP00000347507.3:p.Asn232=
NM_000257.3:c.695A= NP_000248.2:p.Asn232=
XR_245686.3:n.801A=
XM_017021340.1:c.695A= XP_016876829.1:p.Asn232=
NM_000257.4:c.695A= MANE Select NP_000248.2:p.Asn232=