Canonical Allele Identifier: CA2697559422

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10628683G>A , CM000679.2:g.10628683G>A	GRCh38
NC_000017.10:g.10532000G>A , CM000679.1:g.10532000G>A	GRCh37
NC_000017.9:g.10472725G>A	NCBI36
NG_011537.1:g.33616C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002470.4:c.5797-4C>T MANE Select	NP_002461.2:n.5797-4C>T
ENST00000583535.6:c.5797-4C>T MANE Select	ENSP00000464317.1:n.5797-4C>T
NM_002470.3:c.5797-4C>T	NP_002461.2:n.5797-4C>T
ENST00000577963.1:n.339-4C>T
ENST00000579928.2:n.327-4C>T
ENST00000583535.5:c.5797-4C>T	ENSP00000464317.1:n.5797-4C>T
XM_011523870.1:c.5797-4C>T	XP_011522172.1:n.5797-4C>T
XM_011523870.3:c.5797-4C>T	XP_011522172.1:n.5797-4C>T
XM_011523871.1:c.5797-4C>T	XP_011522173.1:n.5797-4C>T
XM_011523871.2:c.5797-4C>T	XP_011522173.1:n.5797-4C>T