Canonical Allele Identifier: CA2123445548
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429100A= , CM000676.2:g.23429100A= GRCh38
NC_000014.8:g.23898309A= , CM000676.1:g.23898309A= GRCh37
NC_000014.7:g.22968149A= NCBI36
NG_007884.1:g.11562T= , LRG_384:g.11562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1262T= MANE Select ENSP00000347507.3:p.Ile421=
ENST00000355349.3:c.1262T= ENSP00000347507.3:p.Ile421=
NM_000257.3:c.1262T= NP_000248.2:p.Ile421=
XR_245686.3:n.1368T=
XM_017021340.1:c.1262T= XP_016876829.1:p.Ile421=
NM_000257.4:c.1262T= MANE Select NP_000248.2:p.Ile421=