Canonical Allele Identifier: CA8392681

Gene: MYH3

Linked Data

• dbSNP Id: rs779438713
• ExAC: 17:10543033 C / T
• gnomAD v2: 17-10543033-C-T
• gnomAD v4: 17-10639716-C-T
• MyVariant Identifiers: chr17:g.10543033C>T (hg19) ; chr17:g.10639716C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639716C>T , CM000679.2:g.10639716C>T	GRCh38
NC_000017.10:g.10543033C>T , CM000679.1:g.10543033C>T	GRCh37
NC_000017.9:g.10483758C>T	NCBI36
NG_011537.1:g.22583G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2769G>A MANE Select	ENSP00000464317.1:p.Val923=
ENST00000583535.5:c.2769G>A	ENSP00000464317.1:p.Val923=
NM_002470.3:c.2769G>A	NP_002461.2:p.Val923=
XM_011523870.1:c.2769G>A	XP_011522172.1:p.Val923=
XM_011523871.1:c.2769G>A	XP_011522173.1:p.Val923=
XM_011523872.1:c.2769G>A	XP_011522174.1:p.Val923=
XM_011523870.3:c.2769G>A	XP_011522172.1:p.Val923=
XM_011523871.2:c.2769G>A	XP_011522173.1:p.Val923=
NM_002470.4:c.2769G>A MANE Select	NP_002461.2:p.Val923=