Canonical Allele Identifier: CA497979351

Gene: MYH3

Linked Data

• dbSNP Id: rs2074249900
• gnomAD v4: 17-10639662-C-T
• MyVariant Identifiers: chr17:g.10542979C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639662C>T , CM000679.2:g.10639662C>T	GRCh38
NC_000017.10:g.10542979C>T , CM000679.1:g.10542979C>T	GRCh37
NC_000017.9:g.10483704C>T	NCBI36
NG_011537.1:g.22637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2823G>A MANE Select	ENSP00000464317.1:p.Lys941=
ENST00000583535.5:c.2823G>A	ENSP00000464317.1:p.Lys941=
NM_002470.3:c.2823G>A	NP_002461.2:p.Lys941=
XM_011523870.1:c.2823G>A	XP_011522172.1:p.Lys941=
XM_011523871.1:c.2823G>A	XP_011522173.1:p.Lys941=
XM_011523872.1:c.2823G>A	XP_011522174.1:p.Lys941=
XM_011523870.3:c.2823G>A	XP_011522172.1:p.Lys941=
XM_011523871.2:c.2823G>A	XP_011522173.1:p.Lys941=
NM_002470.4:c.2823G>A MANE Select	NP_002461.2:p.Lys941=