Canonical Allele Identifier: CA485767253
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1229246
ClinVar RCV Id: RCV001609486
dbSNP Id: rs1313652063
MyVariant Identifiers: chr14:g.23900658T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431449T>A , CM000676.2:g.23431449T>A GRCh38
NC_000014.8:g.23900658T>A , CM000676.1:g.23900658T>A GRCh37
NC_000014.7:g.22970498T>A NCBI36
NG_007884.1:g.9213A>T , LRG_384:g.9213A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.765A>T MANE Select ENSP00000347507.3:p.Thr255=
ENST00000355349.3:c.765A>T ENSP00000347507.3:p.Thr255=
NM_000257.3:c.765A>T NP_000248.2:p.Thr255=
XR_245686.3:n.871A>T
XM_017021340.1:c.765A>T XP_016876829.1:p.Thr255=
NM_000257.4:c.765A>T MANE Select NP_000248.2:p.Thr255=