Canonical Allele Identifier: CA2123455582
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424719A= , CM000676.2:g.23424719A= GRCh38
NC_000014.8:g.23893928A= , CM000676.1:g.23893928A= GRCh37
NC_000014.7:g.22963768A= NCBI36
NG_007884.1:g.15943T= , LRG_384:g.15943T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2679+50T= MANE Select ENSP00000347507.3:n.2679+50T=
ENST00000355349.3:c.2679+50T= ENSP00000347507.3:n.2679+50T=
NM_000257.3:c.2679+50T= NP_000248.2:n.2679+50T=
XR_245686.3:n.2785+50T=
XM_017021340.1:c.2679+50T= XP_016876829.1:n.2679+50T=
NM_000257.4:c.2679+50T= MANE Select NP_000248.2:n.2679+50T=
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