Canonical Allele Identifier: CA2403794869

Gene: MYH9

Linked Data

• dbSNP Id: rs2016494481

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281839dup , CM000684.2:g.36281839dup	GRCh38
NC_000022.10:g.36677885dup , CM000684.1:g.36677885dup	GRCh37
NC_000022.9:g.35007831dup	NCBI36
NG_011884.2:g.111180dup , LRG_567:g.111180dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3145dup
ENST00000685801.1:c.*829dup	ENSP00000510688.1:n.*829dup
ENST00000690244.1:n.2048dup
ENST00000691109.1:n.7007dup
ENST00000216181.11:c.*829dup MANE Select	ENSP00000216181.6:n.*829dup
ENST00000216181.9:c.*829dup	ENSP00000216181.5:n.*829dup
NM_002473.5:c.*829dup , LRG_567t1:c.*829dup	NP_002464.1:n.*829dup
XM_011530197.1:c.*829dup	XP_011528499.1:n.*829dup
XM_011530197.2:c.*829dup	XP_011528499.1:n.*829dup
XM_017028803.1:c.*829dup	XP_016884292.1:n.*829dup
XM_017028804.1:c.*829dup	XP_016884293.1:n.*829dup
XM_017028805.1:c.*829dup	XP_016884294.1:n.*829dup
XM_017028806.1:c.*829dup	XP_016884295.1:n.*829dup
NM_002473.6:c.*829dup MANE Select	NP_002464.1:n.*829dup