Canonical Allele Identifier: CA389052235
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 644163
ClinVar RCV Id: RCV000798023
dbSNP Id: rs730880848

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431620C>T , CM000676.2:g.23431620C>T GRCh38
NC_000014.8:g.23900829C>T , CM000676.1:g.23900829C>T GRCh37
NC_000014.7:g.22970669C>T NCBI36
NG_007884.1:g.9042G>A , LRG_384:g.9042G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.697G>A MANE Select ENSP00000347507.3:p.Ala233Thr
ENST00000355349.3:c.697G>A ENSP00000347507.3:p.Ala233Thr
NM_000257.3:c.697G>A NP_000248.2:p.Ala233Thr
XR_245686.3:n.803G>A
XM_017021340.1:c.697G>A XP_016876829.1:p.Ala233Thr
NM_000257.4:c.697G>A MANE Select NP_000248.2:p.Ala233Thr