Canonical Allele Identifier: CA485766586
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23892876G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423667G>T , CM000676.2:g.23423667G>T GRCh38
NC_000014.8:g.23892876G>T , CM000676.1:g.23892876G>T GRCh37
NC_000014.7:g.22962716G>T NCBI36
NG_007884.1:g.16995C>A , LRG_384:g.16995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2979C>A MANE Select ENSP00000347507.3:p.Thr993=
ENST00000355349.3:c.2979C>A ENSP00000347507.3:p.Thr993=
NM_000257.3:c.2979C>A NP_000248.2:p.Thr993=
XR_245686.3:n.3085C>A
XM_017021340.1:c.2979C>A XP_016876829.1:p.Thr993=
NM_000257.4:c.2979C>A MANE Select NP_000248.2:p.Thr993=
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