Canonical Allele Identifier: CA981429826

Gene: MYH3

Linked Data

• dbSNP Id: rs2074248373
• gnomAD v3: 17-10639495-A-ACT
• gnomAD v4: 17-10639495-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639495_10639496insCT , CM000679.2:g.10639495_10639496insCT	GRCh38
NC_000017.10:g.10542812_10542813insCT , CM000679.1:g.10542812_10542813insCT	GRCh37
NC_000017.9:g.10483537_10483538insCT	NCBI36
NG_011537.1:g.22803_22804insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926-22_2926-21insAG MANE Select	ENSP00000464317.1:n.2926-22_2926-21insAG
ENST00000583535.5:c.2926-22_2926-21insAG	ENSP00000464317.1:n.2926-22_2926-21insAG
NM_002470.3:c.2926-22_2926-21insAG	NP_002461.2:n.2926-22_2926-21insAG
XM_011523870.1:c.2926-22_2926-21insAG	XP_011522172.1:n.2926-22_2926-21insAG
XM_011523871.1:c.2926-22_2926-21insAG	XP_011522173.1:n.2926-22_2926-21insAG
XM_011523872.1:c.2926-22_2926-21insAG	XP_011522174.1:n.2926-22_2926-21insAG
XM_011523870.3:c.2926-22_2926-21insAG	XP_011522172.1:n.2926-22_2926-21insAG
XM_011523871.2:c.2926-22_2926-21insAG	XP_011522173.1:n.2926-22_2926-21insAG
NM_002470.4:c.2926-22_2926-21insAG MANE Select	NP_002461.2:n.2926-22_2926-21insAG