Canonical Allele Identifier: CA389052072
Gene: MYH7 HGNC NCBI

Linked Data

COSMIC: COSM954782
MyVariant Identifiers: chr14:g.23900644G>T (hg19) chr14:g.23431435G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431435G>T , CM000676.2:g.23431435G>T GRCh38
NC_000014.8:g.23900644G>T , CM000676.1:g.23900644G>T GRCh37
NC_000014.7:g.22970484G>T NCBI36
NG_007884.1:g.9227C>A , LRG_384:g.9227C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.779C>A MANE Select ENSP00000347507.3:p.Ser260Tyr
ENST00000355349.3:c.779C>A ENSP00000347507.3:p.Ser260Tyr
NM_000257.3:c.779C>A NP_000248.2:p.Ser260Tyr
XR_245686.3:n.885C>A
XM_017021340.1:c.779C>A XP_016876829.1:p.Ser260Tyr
NM_000257.4:c.779C>A MANE Select NP_000248.2:p.Ser260Tyr
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