Canonical Allele Identifier: CA2123455589
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424732C= , CM000676.2:g.23424732C= GRCh38
NC_000014.8:g.23893941C= , CM000676.1:g.23893941C= GRCh37
NC_000014.7:g.22963781C= NCBI36
NG_007884.1:g.15930G= , LRG_384:g.15930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2679+37G= MANE Select ENSP00000347507.3:n.2679+37G=
ENST00000355349.3:c.2679+37G= ENSP00000347507.3:n.2679+37G=
NM_000257.3:c.2679+37G= NP_000248.2:n.2679+37G=
XR_245686.3:n.2785+37G=
XM_017021340.1:c.2679+37G= XP_016876829.1:n.2679+37G=
NM_000257.4:c.2679+37G= MANE Select NP_000248.2:n.2679+37G=
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