Canonical Allele Identifier: CA2123451116
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431307C= , CM000676.2:g.23431307C= GRCh38
NC_000014.8:g.23900516C= , CM000676.1:g.23900516C= GRCh37
NC_000014.7:g.22970356C= NCBI36
NG_007884.1:g.9355G= , LRG_384:g.9355G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+111G= MANE Select ENSP00000347507.3:n.796+111G=
ENST00000355349.3:c.796+111G= ENSP00000347507.3:n.796+111G=
NM_000257.3:c.796+111G= NP_000248.2:n.796+111G=
XR_245686.3:n.902+111G=
XM_017021340.1:c.796+111G= XP_016876829.1:n.796+111G=
NM_000257.4:c.796+111G= MANE Select NP_000248.2:n.796+111G=
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