Canonical Allele Identifier: CA497979398

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639689-C-T
• MyVariant Identifiers: chr17:g.10543006C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639689C>T , CM000679.2:g.10639689C>T	GRCh38
NC_000017.10:g.10543006C>T , CM000679.1:g.10543006C>T	GRCh37
NC_000017.9:g.10483731C>T	NCBI36
NG_011537.1:g.22610G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2796G>A MANE Select	ENSP00000464317.1:p.Glu932=
ENST00000583535.5:c.2796G>A	ENSP00000464317.1:p.Glu932=
NM_002470.3:c.2796G>A	NP_002461.2:p.Glu932=
XM_011523870.1:c.2796G>A	XP_011522172.1:p.Glu932=
XM_011523871.1:c.2796G>A	XP_011522173.1:p.Glu932=
XM_011523872.1:c.2796G>A	XP_011522174.1:p.Glu932=
XM_011523870.3:c.2796G>A	XP_011522172.1:p.Glu932=
XM_011523871.2:c.2796G>A	XP_011522173.1:p.Glu932=
NM_002470.4:c.2796G>A MANE Select	NP_002461.2:p.Glu932=