Canonical Allele Identifier: CA485766775
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2845623
ClinVar RCV Id: RCV003750176
MyVariant Identifiers: chr14:g.23893125T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423916T>C , CM000676.2:g.23423916T>C GRCh38
NC_000014.8:g.23893125T>C , CM000676.1:g.23893125T>C GRCh37
NC_000014.7:g.22962965T>C NCBI36
NG_007884.1:g.16746A>G , LRG_384:g.16746A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2913A>G MANE Select ENSP00000347507.3:p.Thr971=
ENST00000355349.3:c.2913A>G ENSP00000347507.3:p.Thr971=
NM_000257.3:c.2913A>G NP_000248.2:p.Thr971=
XR_245686.3:n.3019A>G
XM_017021340.1:c.2913A>G XP_016876829.1:p.Thr971=
NM_000257.4:c.2913A>G MANE Select NP_000248.2:p.Thr971=