Canonical Allele Identifier: CA2123444885
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419396G= , CM000676.2:g.23419396G= GRCh38
NC_000014.8:g.23888605G= , CM000676.1:g.23888605G= GRCh37
NC_000014.7:g.22958445G= NCBI36
NG_007884.1:g.21266C= , LRG_384:g.21266C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3853+87C= MANE Select ENSP00000347507.3:n.3853+87C=
ENST00000355349.3:c.3853+87C= ENSP00000347507.3:n.3853+87C=
NM_000257.3:c.3853+87C= NP_000248.2:n.3853+87C=
XM_017021340.1:c.3853+87C= XP_016876829.1:n.3853+87C=
NM_000257.4:c.3853+87C= MANE Select NP_000248.2:n.3853+87C=