Canonical Allele Identifier: CA2123455959
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433663G= , CM000676.2:g.23433663G= GRCh38
NC_000014.8:g.23902872G= , CM000676.1:g.23902872G= GRCh37
NC_000014.7:g.22972712G= NCBI36
NG_007884.1:g.6999C= , LRG_384:g.6999C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.70C= MANE Select ENSP00000347507.3:p.Leu24=
ENST00000355349.3:c.70C= ENSP00000347507.3:p.Leu24=
NM_000257.3:c.70C= NP_000248.2:p.Leu24=
XR_245686.3:n.176C=
XM_017021340.1:c.70C= XP_016876829.1:p.Leu24=
NM_000257.4:c.70C= MANE Select NP_000248.2:p.Leu24=