Canonical Allele Identifier: CA1025462272

Gene: MYH9

Linked Data

• dbSNP Id: rs2016492399
• gnomAD v3: 22-36281775-CA-C
• gnomAD v4: 22-36281775-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281776del , CM000684.2:g.36281776del	GRCh38
NC_000022.10:g.36677822del , CM000684.1:g.36677822del	GRCh37
NC_000022.9:g.35007768del	NCBI36
NG_011884.2:g.111243del , LRG_567:g.111243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3208del
ENST00000685801.1:c.*892del	ENSP00000510688.1:n.*892del
ENST00000690244.1:n.2111del
ENST00000691109.1:n.7070del
ENST00000216181.11:c.*892del MANE Select	ENSP00000216181.6:n.*892del
ENST00000216181.9:c.*892del	ENSP00000216181.5:n.*892del
NM_002473.5:c.*892del , LRG_567t1:c.*892del	NP_002464.1:n.*892del
XM_011530197.1:c.*892del	XP_011528499.1:n.*892del
XM_011530197.2:c.*892del	XP_011528499.1:n.*892del
XM_017028803.1:c.*892del	XP_016884292.1:n.*892del
XM_017028804.1:c.*892del	XP_016884293.1:n.*892del
XM_017028805.1:c.*892del	XP_016884294.1:n.*892del
XM_017028806.1:c.*892del	XP_016884295.1:n.*892del
NM_002473.6:c.*892del MANE Select	NP_002464.1:n.*892del