Canonical Allele Identifier: CA2123441220
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417625A= , CM000676.2:g.23417625A= GRCh38
NC_000014.8:g.23886834A= , CM000676.1:g.23886834A= GRCh37
NC_000014.7:g.22956674A= NCBI36
NG_007884.1:g.23037T= , LRG_384:g.23037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4231T= MANE Select ENSP00000347507.3:p.Cys1411=
ENST00000355349.3:c.4231T= ENSP00000347507.3:p.Cys1411=
NM_000257.3:c.4231T= NP_000248.2:p.Cys1411=
XM_017021340.1:c.4231T= XP_016876829.1:p.Cys1411=
NM_000257.4:c.4231T= MANE Select NP_000248.2:p.Cys1411=