Canonical Allele Identifier: CA2123445826
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429196T= , CM000676.2:g.23429196T= GRCh38
NC_000014.8:g.23898405T= , CM000676.1:g.23898405T= GRCh37
NC_000014.7:g.22968245T= NCBI36
NG_007884.1:g.11466A= , LRG_384:g.11466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1257+33A= MANE Select ENSP00000347507.3:n.1257+33A=
ENST00000355349.3:c.1257+33A= ENSP00000347507.3:n.1257+33A=
NM_000257.3:c.1257+33A= NP_000248.2:n.1257+33A=
XR_245686.3:n.1363+33A=
XM_017021340.1:c.1257+33A= XP_016876829.1:n.1257+33A=
NM_000257.4:c.1257+33A= MANE Select NP_000248.2:n.1257+33A=