Canonical Allele Identifier: CA2403794867

Gene: MYH9

Linked Data

• dbSNP Id: rs2016494435
• gnomAD v4: 22-36281837-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281838del , CM000684.2:g.36281838del	GRCh38
NC_000022.10:g.36677884del , CM000684.1:g.36677884del	GRCh37
NC_000022.9:g.35007830del	NCBI36
NG_011884.2:g.111181del , LRG_567:g.111181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3146del
ENST00000685801.1:c.*830del	ENSP00000510688.1:n.*830del
ENST00000690244.1:n.2049del
ENST00000691109.1:n.7008del
ENST00000216181.11:c.*830del MANE Select	ENSP00000216181.6:n.*830del
ENST00000216181.9:c.*830del	ENSP00000216181.5:n.*830del
NM_002473.5:c.*830del , LRG_567t1:c.*830del	NP_002464.1:n.*830del
XM_011530197.1:c.*830del	XP_011528499.1:n.*830del
XM_011530197.2:c.*830del	XP_011528499.1:n.*830del
XM_017028803.1:c.*830del	XP_016884292.1:n.*830del
XM_017028804.1:c.*830del	XP_016884293.1:n.*830del
XM_017028805.1:c.*830del	XP_016884294.1:n.*830del
XM_017028806.1:c.*830del	XP_016884295.1:n.*830del
NM_002473.6:c.*830del MANE Select	NP_002464.1:n.*830del