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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2123441755
Community Standard Title: NM_000257.4(MYH7):c.1816G= (p.Val606=)
Gene: MYH7
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23427657C= , CM000676.2:g.23427657C=
GRCh38
NC_000014.8:g.23896866C= , CM000676.1:g.23896866C=
GRCh37
NC_000014.7:g.22966706C=
NCBI36
NG_007884.1:g.13005G= , LRG_384:g.13005G=
Transcript Alleles
HGVS
Amino-acid Change
NM_000257.4:c.1816G=
MANE Select
NP_000248.2:p.Val606=
ENST00000355349.4:c.1816G=
MANE Select
ENSP00000347507.3:p.Val606=
NM_000257.3:c.1816G=
NP_000248.2:p.Val606=
ENST00000355349.3:c.1816G=
ENSP00000347507.3:p.Val606=
XM_017021340.1:c.1816G=
XP_016876829.1:p.Val606=
XR_245686.3:n.1922G=
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