Canonical Allele Identifier: CA2739446793
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419816T>A , CM000676.2:g.23419816T>A GRCh38
NC_000014.8:g.23889025T>A , CM000676.1:g.23889025T>A GRCh37
NC_000014.7:g.22958865T>A NCBI36
NG_007884.1:g.20846A>T , LRG_384:g.20846A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3726+29A>T MANE Select ENSP00000347507.3:n.3726+29A>T
ENST00000355349.3:c.3726+29A>T ENSP00000347507.3:n.3726+29A>T
NM_000257.3:c.3726+29A>T NP_000248.2:n.3726+29A>T
XM_017021340.1:c.3726+29A>T XP_016876829.1:n.3726+29A>T
NM_000257.4:c.3726+29A>T MANE Select NP_000248.2:n.3726+29A>T
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