Canonical Allele Identifier: CA485765859
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2919159
ClinVar RCV Id: RCV003749767
MyVariant Identifiers: chr14:g.23884438G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415229G>A , CM000676.2:g.23415229G>A GRCh38
NC_000014.8:g.23884438G>A , CM000676.1:g.23884438G>A GRCh37
NC_000014.7:g.22954278G>A NCBI36
NG_007884.1:g.25433C>T , LRG_384:g.25433C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5325C>T MANE Select ENSP00000347507.3:p.Thr1775=
ENST00000355349.3:c.5325C>T ENSP00000347507.3:p.Thr1775=
NM_000257.3:c.5325C>T NP_000248.2:p.Thr1775=
XM_017021340.1:c.5325C>T XP_016876829.1:p.Thr1775=
NM_000257.4:c.5325C>T MANE Select NP_000248.2:p.Thr1775=
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