Canonical Allele Identifier: CA398155848

Gene: MYH3

Linked Data

• MyVariant Identifiers: chr17:g.10542714T>A (hg19) ; chr17:g.10639397T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639397T>A , CM000679.2:g.10639397T>A	GRCh38
NC_000017.10:g.10542714T>A , CM000679.1:g.10542714T>A	GRCh37
NC_000017.9:g.10483439T>A	NCBI36
NG_011537.1:g.22902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.3003A>T MANE Select	ENSP00000464317.1:p.Gln1001His
ENST00000583535.5:c.3003A>T	ENSP00000464317.1:p.Gln1001His
NM_002470.3:c.3003A>T	NP_002461.2:p.Gln1001His
XM_011523870.1:c.3003A>T	XP_011522172.1:p.Gln1001His
XM_011523871.1:c.3003A>T	XP_011522173.1:p.Gln1001His
XM_011523872.1:c.3003A>T	XP_011522174.1:p.Gln1001His
XM_011523870.3:c.3003A>T	XP_011522172.1:p.Gln1001His
XM_011523871.2:c.3003A>T	XP_011522173.1:p.Gln1001His
NM_002470.4:c.3003A>T MANE Select	NP_002461.2:p.Gln1001His