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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2123445153
Community Standard Title: NM_000257.4(MYH7):c.1357C= (p.Arg453=)
Gene: MYH7
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23429005G= , CM000676.2:g.23429005G=
GRCh38
NC_000014.8:g.23898214G= , CM000676.1:g.23898214G=
GRCh37
NC_000014.7:g.22968054G=
NCBI36
NG_007884.1:g.11657C= , LRG_384:g.11657C=
Transcript Alleles
HGVS
Amino-acid Change
NM_000257.4:c.1357C=
MANE Select
NP_000248.2:p.Arg453=
ENST00000355349.4:c.1357C=
MANE Select
ENSP00000347507.3:p.Arg453=
NM_000257.3:c.1357C=
NP_000248.2:p.Arg453=
ENST00000355349.3:c.1357C=
ENSP00000347507.3:p.Arg453=
XM_017021340.1:c.1357C=
XP_016876829.1:p.Arg453=
XR_245686.3:n.1463C=
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