Canonical Allele Identifier: CA2247333622

Gene: MYH3

Linked Data

• dbSNP Id: rs2074251501
• gnomAD v4: 17-10639807-A-AAAAAAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639810_10639818dup , CM000679.2:g.10639810_10639818dup	GRCh38
NC_000017.10:g.10543127_10543135dup , CM000679.1:g.10543127_10543135dup	GRCh37
NC_000017.9:g.10483852_10483860dup	NCBI36
NG_011537.1:g.22483_22491dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2683-14_2683-6dup MANE Select	ENSP00000464317.1:n.2683-14_2683-6dup
ENST00000583535.5:c.2683-14_2683-6dup	ENSP00000464317.1:n.2683-14_2683-6dup
NM_002470.3:c.2683-14_2683-6dup	NP_002461.2:n.2683-14_2683-6dup
XM_011523870.1:c.2683-14_2683-6dup	XP_011522172.1:n.2683-14_2683-6dup
XM_011523871.1:c.2683-14_2683-6dup	XP_011522173.1:n.2683-14_2683-6dup
XM_011523872.1:c.2683-14_2683-6dup	XP_011522174.1:n.2683-14_2683-6dup
XM_011523870.3:c.2683-14_2683-6dup	XP_011522172.1:n.2683-14_2683-6dup
XM_011523871.2:c.2683-14_2683-6dup	XP_011522173.1:n.2683-14_2683-6dup
NM_002470.4:c.2683-14_2683-6dup MANE Select	NP_002461.2:n.2683-14_2683-6dup