Canonical Allele Identifier: CA2123453730
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423846G= , CM000676.2:g.23423846G= GRCh38
NC_000014.8:g.23893055G= , CM000676.1:g.23893055G= GRCh37
NC_000014.7:g.22962895G= NCBI36
NG_007884.1:g.16816C= , LRG_384:g.16816C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2922+61C= MANE Select ENSP00000347507.3:n.2922+61C=
ENST00000355349.3:c.2922+61C= ENSP00000347507.3:n.2922+61C=
NM_000257.3:c.2922+61C= NP_000248.2:n.2922+61C=
XR_245686.3:n.3028+61C=
XM_017021340.1:c.2922+61C= XP_016876829.1:n.2922+61C=
NM_000257.4:c.2922+61C= MANE Select NP_000248.2:n.2922+61C=
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