Canonical Allele Identifier: CA2123455605
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424745C= , CM000676.2:g.23424745C= GRCh38
NC_000014.8:g.23893954C= , CM000676.1:g.23893954C= GRCh37
NC_000014.7:g.22963794C= NCBI36
NG_007884.1:g.15917G= , LRG_384:g.15917G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2679+24G= MANE Select ENSP00000347507.3:n.2679+24G=
ENST00000355349.3:c.2679+24G= ENSP00000347507.3:n.2679+24G=
NM_000257.3:c.2679+24G= NP_000248.2:n.2679+24G=
XR_245686.3:n.2785+24G=
XM_017021340.1:c.2679+24G= XP_016876829.1:n.2679+24G=
NM_000257.4:c.2679+24G= MANE Select NP_000248.2:n.2679+24G=
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