Canonical Allele Identifier: CA485766679
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23889165C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419956C>T , CM000676.2:g.23419956C>T GRCh38
NC_000014.8:g.23889165C>T , CM000676.1:g.23889165C>T GRCh37
NC_000014.7:g.22959005C>T NCBI36
NG_007884.1:g.20706G>A , LRG_384:g.20706G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.3615G>A MANE Select ENSP00000347507.3:p.Glu1205=
ENST00000355349.3:c.3615G>A ENSP00000347507.3:p.Glu1205=
NM_000257.3:c.3615G>A NP_000248.2:p.Glu1205=
XM_017021340.1:c.3615G>A XP_016876829.1:p.Glu1205=
NM_000257.4:c.3615G>A MANE Select NP_000248.2:p.Glu1205=
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