Canonical Allele Identifier: CA752843306

Gene: MYH9

Linked Data

• dbSNP Id: rs136203
• gnomAD v3: 22-36354956-AACACAC-A
• gnomAD v4: 22-36354956-AACACAC-A
• MyVariant Identifiers: chr22:g.36751002_36751007del (hg19) ; chr22:g.36354957_36354962del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36354996_36355001del , CM000684.2:g.36354996_36355001del	GRCh38
NC_000022.10:g.36751041_36751046del , CM000684.1:g.36751041_36751046del	GRCh37
NC_000022.9:g.35080987_35080992del	NCBI36
NG_011884.2:g.38057_38062del , LRG_567:g.38057_38062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.196-5707_196-5702del
ENST00000685191.1:n.205-5707_205-5702del
ENST00000685801.1:c.-19-5707_-19-5702del	ENSP00000510688.1:n.-19-5707_-19-5702del
ENST00000688137.1:c.-19-5707_-19-5702del	ENSP00000510189.1:n.-19-5707_-19-5702del
ENST00000691296.1:c.-19-5707_-19-5702del	ENSP00000509816.1:n.-19-5707_-19-5702del
ENST00000691687.1:n.196-5707_196-5702del
ENST00000692930.1:n.196-5707_196-5702del
ENST00000216181.11:c.-19-5707_-19-5702del MANE Select	ENSP00000216181.6:n.-19-5707_-19-5702del
ENST00000216181.9:c.-19-5707_-19-5702del	ENSP00000216181.5:n.-19-5707_-19-5702del
ENST00000401701.1:c.-19-5707_-19-5702del	ENSP00000384631.1:n.-19-5707_-19-5702del
ENST00000456729.1:c.-19-5707_-19-5702del	ENSP00000414852.1:n.-19-5707_-19-5702del
NM_002473.5:c.-19-5707_-19-5702del , LRG_567t1:c.-19-5707_-19-5702del	NP_002464.1:n.-19-5707_-19-5702del
XM_011530197.1:c.-19-5707_-19-5702del	XP_011528499.1:n.-19-5707_-19-5702del
XM_011530197.2:c.-19-5707_-19-5702del	XP_011528499.1:n.-19-5707_-19-5702del
XM_017028803.1:c.-19-5707_-19-5702del	XP_016884292.1:n.-19-5707_-19-5702del
XM_017028804.1:c.-19-5707_-19-5702del	XP_016884293.1:n.-19-5707_-19-5702del
XM_017028806.1:c.-19-5707_-19-5702del	XP_016884295.1:n.-19-5707_-19-5702del
NM_002473.6:c.-19-5707_-19-5702del MANE Select	NP_002464.1:n.-19-5707_-19-5702del