Canonical Allele Identifier: CA287776956

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10629607G>A , CM000679.2:g.10629607G>A	GRCh38
NC_000017.10:g.10532924G>A , CM000679.1:g.10532924G>A	GRCh37
NC_000017.9:g.10473649G>A	NCBI36
NG_011537.1:g.32692C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002470.4:c.5786C>T MANE Select	NP_002461.2:p.Thr1929Ile
ENST00000583535.6:c.5786C>T MANE Select	ENSP00000464317.1:p.Thr1929Ile
NM_002470.3:c.5786C>T	NP_002461.2:p.Thr1929Ile
ENST00000577963.1:n.328C>T
ENST00000579928.2:n.316C>T
ENST00000583535.5:c.5786C>T	ENSP00000464317.1:p.Thr1929Ile
XM_011523870.1:c.5786C>T	XP_011522172.1:p.Thr1929Ile
XM_011523870.3:c.5786C>T	XP_011522172.1:p.Thr1929Ile
XM_011523871.1:c.5786C>T	XP_011522173.1:p.Thr1929Ile
XM_011523871.2:c.5786C>T	XP_011522173.1:p.Thr1929Ile