Canonical Allele Identifier: CA2123445757
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419706G= , CM000676.2:g.23419706G= GRCh38
NC_000014.8:g.23888915G= , CM000676.1:g.23888915G= GRCh37
NC_000014.7:g.22958755G= NCBI36
NG_007884.1:g.20956C= , LRG_384:g.20956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3727-97C= MANE Select ENSP00000347507.3:n.3727-97C=
ENST00000355349.3:c.3727-97C= ENSP00000347507.3:n.3727-97C=
NM_000257.3:c.3727-97C= NP_000248.2:n.3727-97C=
XM_017021340.1:c.3727-97C= XP_016876829.1:n.3727-97C=
NM_000257.4:c.3727-97C= MANE Select NP_000248.2:n.3727-97C=