Canonical Allele Identifier: CA2695219243
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419296dup , CM000676.2:g.23419296dup GRCh38
NC_000014.8:g.23888505dup , CM000676.1:g.23888505dup GRCh37
NC_000014.7:g.22958345dup NCBI36
NG_007884.1:g.21367dup , LRG_384:g.21367dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3854dup
ENST00000355349.3:c.3854dup
NM_000257.3:c.3854dup
XM_017021340.1:c.3854dup
NM_000257.4:c.3854dup