Canonical Allele Identifier: CA485621837
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1658340
ClinVar RCV Id: RCV002171909
dbSNP Id: rs747198710
MyVariant Identifiers: chr14:g.23891466C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422257C>T , CM000676.2:g.23422257C>T GRCh38
NC_000014.8:g.23891466C>T , CM000676.1:g.23891466C>T GRCh37
NC_000014.7:g.22961306C>T NCBI36
NG_007884.1:g.18405G>A , LRG_384:g.18405G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3168G>A MANE Select ENSP00000347507.3:p.Glu1056=
ENST00000355349.3:c.3168G>A ENSP00000347507.3:p.Glu1056=
NM_000257.3:c.3168G>A NP_000248.2:p.Glu1056=
XR_245686.3:n.3274G>A
XM_017021340.1:c.3168G>A XP_016876829.1:p.Glu1056=
NM_000257.4:c.3168G>A MANE Select NP_000248.2:p.Glu1056=