Canonical Allele Identifier: CA725974985

Gene: MYH3

Linked Data

• dbSNP Id: rs1410581366
• gnomAD v3: 17-10639491-AGC-A
• gnomAD v4: 17-10639491-AGC-A
• MyVariant Identifiers: chr17:g.10542809_10542810del (hg19) ; chr17:g.10639492_10639493del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639492_10639493del , CM000679.2:g.10639492_10639493del	GRCh38
NC_000017.10:g.10542809_10542810del , CM000679.1:g.10542809_10542810del	GRCh37
NC_000017.9:g.10483534_10483535del	NCBI36
NG_011537.1:g.22806_22807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926-19_2926-18del MANE Select	ENSP00000464317.1:n.2926-19_2926-18del
ENST00000583535.5:c.2926-19_2926-18del	ENSP00000464317.1:n.2926-19_2926-18del
NM_002470.3:c.2926-19_2926-18del	NP_002461.2:n.2926-19_2926-18del
XM_011523870.1:c.2926-19_2926-18del	XP_011522172.1:n.2926-19_2926-18del
XM_011523871.1:c.2926-19_2926-18del	XP_011522173.1:n.2926-19_2926-18del
XM_011523872.1:c.2926-19_2926-18del	XP_011522174.1:n.2926-19_2926-18del
XM_011523870.3:c.2926-19_2926-18del	XP_011522172.1:n.2926-19_2926-18del
XM_011523871.2:c.2926-19_2926-18del	XP_011522173.1:n.2926-19_2926-18del
NM_002470.4:c.2926-19_2926-18del MANE Select	NP_002461.2:n.2926-19_2926-18del