Canonical Allele Identifier: CA497979205

Gene: MYH3

Linked Data

• MyVariant Identifiers: chr17:g.10542916C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639599C>A , CM000679.2:g.10639599C>A	GRCh38
NC_000017.10:g.10542916C>A , CM000679.1:g.10542916C>A	GRCh37
NC_000017.9:g.10483641C>A	NCBI36
NG_011537.1:g.22700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2886G>T MANE Select	ENSP00000464317.1:p.Leu962=
ENST00000583535.5:c.2886G>T	ENSP00000464317.1:p.Leu962=
NM_002470.3:c.2886G>T	NP_002461.2:p.Leu962=
XM_011523870.1:c.2886G>T	XP_011522172.1:p.Leu962=
XM_011523871.1:c.2886G>T	XP_011522173.1:p.Leu962=
XM_011523872.1:c.2886G>T	XP_011522174.1:p.Leu962=
XM_011523870.3:c.2886G>T	XP_011522172.1:p.Leu962=
XM_011523871.2:c.2886G>T	XP_011522173.1:p.Leu962=
NM_002470.4:c.2886G>T MANE Select	NP_002461.2:p.Leu962=