Canonical Allele Identifier: CA10577514
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 234707
ClinVar RCV Id: RCV000213114
dbSNP Id: rs876661175

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431765C>T , CM000676.2:g.23431765C>T GRCh38
NC_000014.8:g.23900974C>T , CM000676.1:g.23900974C>T GRCh37
NC_000014.7:g.22970814C>T NCBI36
NG_007884.1:g.8897G>A , LRG_384:g.8897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.635G>A MANE Select ENSP00000347507.3:p.Gly212Asp
ENST00000355349.3:c.635G>A ENSP00000347507.3:p.Gly212Asp
NM_000257.3:c.635G>A NP_000248.2:p.Gly212Asp
XR_245686.3:n.741G>A
XM_017021340.1:c.635G>A XP_016876829.1:p.Gly212Asp
NM_000257.4:c.635G>A MANE Select NP_000248.2:p.Gly212Asp