Canonical Allele Identifier: CA2123449090
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1566528616

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421174dup , CM000676.2:g.23421174dup GRCh38
NC_000014.8:g.23890383dup , CM000676.1:g.23890383dup GRCh37
NC_000014.7:g.22960223dup NCBI36
NG_007884.1:g.19492dup , LRG_384:g.19492dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-122dup MANE Select ENSP00000347507.3:n.3246-122dup
ENST00000355349.3:c.3246-122dup ENSP00000347507.3:n.3246-122dup
NM_000257.3:c.3246-122dup NP_000248.2:n.3246-122dup
XR_245686.3:n.3354-122dup
XM_017021340.1:c.3246-122dup XP_016876829.1:n.3246-122dup
NM_000257.4:c.3246-122dup MANE Select NP_000248.2:n.3246-122dup