Canonical Allele Identifier: CA752830234

Gene: MYH9

Linked Data

• dbSNP Id: rs1446676933
• gnomAD v4: 22-36281814-TGG-T
• MyVariant Identifiers: chr22:g.36677861_36677862del (hg19) ; chr22:g.36281815_36281816del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281815_36281816del , CM000684.2:g.36281815_36281816del	GRCh38
NC_000022.10:g.36677861_36677862del , CM000684.1:g.36677861_36677862del	GRCh37
NC_000022.9:g.35007807_35007808del	NCBI36
NG_011884.2:g.111203_111204del , LRG_567:g.111203_111204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3168_3169del
ENST00000685801.1:c.*852_*853del	ENSP00000510688.1:n.*852_*853del
ENST00000690244.1:n.2071_2072del
ENST00000691109.1:n.7030_7031del
ENST00000216181.11:c.*852_*853del MANE Select	ENSP00000216181.6:n.*852_*853del
ENST00000216181.9:c.*852_*853del	ENSP00000216181.5:n.*852_*853del
NM_002473.5:c.*852_*853del , LRG_567t1:c.*852_*853del	NP_002464.1:n.*852_*853del
XM_011530197.1:c.*852_*853del	XP_011528499.1:n.*852_*853del
XM_011530197.2:c.*852_*853del	XP_011528499.1:n.*852_*853del
XM_017028803.1:c.*852_*853del	XP_016884292.1:n.*852_*853del
XM_017028804.1:c.*852_*853del	XP_016884293.1:n.*852_*853del
XM_017028805.1:c.*852_*853del	XP_016884294.1:n.*852_*853del
XM_017028806.1:c.*852_*853del	XP_016884295.1:n.*852_*853del
NM_002473.6:c.*852_*853del MANE Select	NP_002464.1:n.*852_*853del