Canonical Allele Identifier: CA257818034
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs36061260

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422461dup , CM000676.2:g.23422461dup GRCh38
NC_000014.8:g.23891670dup , CM000676.1:g.23891670dup GRCh37
NC_000014.7:g.22961510dup NCBI36
NG_007884.1:g.18201dup , LRG_384:g.18201dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-136dup MANE Select ENSP00000347507.3:n.3100-136dup
ENST00000355349.3:c.3100-136dup ENSP00000347507.3:n.3100-136dup
NM_000257.3:c.3100-136dup NP_000248.2:n.3100-136dup
XR_245686.3:n.3206-136dup
XM_017021340.1:c.3100-136dup XP_016876829.1:n.3100-136dup
NM_000257.4:c.3100-136dup MANE Select NP_000248.2:n.3100-136dup