Canonical Allele Identifier: CA752830170

Gene: MYH9

Linked Data

• dbSNP Id: rs1368162237
• gnomAD v3: 22-36281746-C-CA
• gnomAD v4: 22-36281746-C-CA
• MyVariant Identifiers: chr22:g.36677792_36677793insA (hg19) ; chr22:g.36281746_36281747insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281748dup , CM000684.2:g.36281748dup	GRCh38
NC_000022.10:g.36677794dup , CM000684.1:g.36677794dup	GRCh37
NC_000022.9:g.35007740dup	NCBI36
NG_011884.2:g.111272dup , LRG_567:g.111272dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3237dup
ENST00000685801.1:c.*921dup	ENSP00000510688.1:n.*921dup
ENST00000690244.1:n.2140dup
ENST00000691109.1:n.7099dup
ENST00000216181.11:c.*921dup MANE Select	ENSP00000216181.6:n.*921dup
ENST00000216181.9:c.*921dup	ENSP00000216181.5:n.*921dup
NM_002473.5:c.*921dup , LRG_567t1:c.*921dup	NP_002464.1:n.*921dup
XM_011530197.1:c.*921dup	XP_011528499.1:n.*921dup
XM_011530197.2:c.*921dup	XP_011528499.1:n.*921dup
XM_017028803.1:c.*921dup	XP_016884292.1:n.*921dup
XM_017028804.1:c.*921dup	XP_016884293.1:n.*921dup
XM_017028805.1:c.*921dup	XP_016884294.1:n.*921dup
XM_017028806.1:c.*921dup	XP_016884295.1:n.*921dup
NM_002473.6:c.*921dup MANE Select	NP_002464.1:n.*921dup