Canonical Allele Identifier: CA913191041

Gene: MYH3

Linked Data

• ClinVar Variation Id: 634845
• ClinVar RCV Id: RCV000785650

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10638956_10645576del , CM000679.2:g.10638956_10645576del	GRCh38
NC_000017.10:g.10542273_10548893del , CM000679.1:g.10542273_10548893del	GRCh37
NC_000017.9:g.10482998_10489618del	NCBI36
NG_011537.1:g.16723_23343del

Transcript Alleles

HGVS	Amino-acid change
ENST00000583535.6:c.1141+131_3256del
ENST00000583535.5:c.1141+131_3256del
NM_002470.3:c.1141+131_3256del
XM_011523870.1:c.1141+131_3256del
XM_011523871.1:c.1141+131_3256del
XM_011523872.1:c.1141+131_3256del
XM_011523870.3:c.1141+131_3256del
XM_011523871.2:c.1141+131_3256del
NM_002470.4:c.1141+131_3256del