Canonical Allele Identifier: CA2123462914
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415369T= , CM000676.2:g.23415369T= GRCh38
NC_000014.8:g.23884578T= , CM000676.1:g.23884578T= GRCh37
NC_000014.7:g.22954418T= NCBI36
NG_007884.1:g.25293A= , LRG_384:g.25293A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5283+12A= MANE Select ENSP00000347507.3:n.5283+12A=
ENST00000355349.3:c.5283+12A= ENSP00000347507.3:n.5283+12A=
NM_000257.3:c.5283+12A= NP_000248.2:n.5283+12A=
XM_017021340.1:c.5283+12A= XP_016876829.1:n.5283+12A=
NM_000257.4:c.5283+12A= MANE Select NP_000248.2:n.5283+12A=
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