Canonical Allele Identifier: CA485765942
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069885
ClinVar RCV Id: RCV004009917
dbSNP Id: rs1327209075
MyVariant Identifiers: chr14:g.23884294C>T (hg19) chr14:g.23415085C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415085C>T , CM000676.2:g.23415085C>T GRCh38
NC_000014.8:g.23884294C>T , CM000676.1:g.23884294C>T GRCh37
NC_000014.7:g.22954134C>T NCBI36
NG_007884.1:g.25577G>A , LRG_384:g.25577G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5469G>A MANE Select ENSP00000347507.3:p.Glu1823=
ENST00000355349.3:c.5469G>A ENSP00000347507.3:p.Glu1823=
NM_000257.3:c.5469G>A NP_000248.2:p.Glu1823=
XM_017021340.1:c.5469G>A XP_016876829.1:p.Glu1823=
NM_000257.4:c.5469G>A MANE Select NP_000248.2:p.Glu1823=
Search 100 bp 5'
Search 100 bp 3'