Canonical Allele Identifier: CA752830473

Gene: MYH9

Linked Data

• dbSNP Id: rs1203665095
• gnomAD v3: 22-36282079-C-CA
• gnomAD v4: 22-36282079-C-CA
• MyVariant Identifiers: chr22:g.36678125_36678126insA (hg19) ; chr22:g.36282079_36282080insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282080dup , CM000684.2:g.36282080dup	GRCh38
NC_000022.10:g.36678126dup , CM000684.1:g.36678126dup	GRCh37
NC_000022.9:g.35008072dup	NCBI36
NG_011884.2:g.110939dup , LRG_567:g.110939dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2904dup
ENST00000685801.1:c.*588dup	ENSP00000510688.1:n.*588dup
ENST00000690244.1:n.1807dup
ENST00000691109.1:n.6766dup
ENST00000216181.11:c.*588dup MANE Select	ENSP00000216181.6:n.*588dup
ENST00000216181.9:c.*588dup	ENSP00000216181.5:n.*588dup
NM_002473.5:c.*588dup , LRG_567t1:c.*588dup	NP_002464.1:n.*588dup
XM_011530197.1:c.*588dup	XP_011528499.1:n.*588dup
XM_011530197.2:c.*588dup	XP_011528499.1:n.*588dup
XM_017028803.1:c.*588dup	XP_016884292.1:n.*588dup
XM_017028804.1:c.*588dup	XP_016884293.1:n.*588dup
XM_017028805.1:c.*588dup	XP_016884294.1:n.*588dup
XM_017028806.1:c.*588dup	XP_016884295.1:n.*588dup
NM_002473.6:c.*588dup MANE Select	NP_002464.1:n.*588dup