Canonical Allele Identifier: CA2247333064

Gene: MYH3

Linked Data

• ClinVar Variation Id: 2200781
• ClinVar RCV Id: RCV002638384
• dbSNP Id: rs2074248065

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639475del , CM000679.2:g.10639475del	GRCh38
NC_000017.10:g.10542792del , CM000679.1:g.10542792del	GRCh37
NC_000017.9:g.10483517del	NCBI36
NG_011537.1:g.22825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926del
ENST00000583535.5:c.2926del
NM_002470.3:c.2926del
XM_011523870.1:c.2926del
XM_011523871.1:c.2926del
XM_011523872.1:c.2926del
XM_011523870.3:c.2926del
XM_011523871.2:c.2926del
NM_002470.4:c.2926del