Canonical Allele Identifier: CA012887
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181201
ClinVar RCV Id: RCV000158563 RCV001857567
dbSNP Id: rs730880755
MyVariant Identifiers: chr14:g.23893338A>T (hg19) chr14:g.23424129A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424129A>T , CM000676.2:g.23424129A>T GRCh38
NC_000014.8:g.23893338A>T , CM000676.1:g.23893338A>T GRCh37
NC_000014.7:g.22963178A>T NCBI36
NG_007884.1:g.16533T>A , LRG_384:g.16533T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2700T>A MANE Select ENSP00000347507.3:p.Asp900Glu
ENST00000355349.3:c.2700T>A ENSP00000347507.3:p.Asp900Glu
NM_000257.3:c.2700T>A NP_000248.2:p.Asp900Glu
XR_245686.3:n.2806T>A
XM_017021340.1:c.2700T>A XP_016876829.1:p.Asp900Glu
NM_000257.4:c.2700T>A MANE Select NP_000248.2:p.Asp900Glu
Search 100 bp 5'
Search 100 bp 3'