Canonical Allele Identifier: CA2403803496

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36299294G= , CM000684.2:g.36299294G=	GRCh38
NC_000022.10:g.36695340G= , CM000684.1:g.36695340G=	GRCh37
NC_000022.9:g.35025286G=	NCBI36
NG_011884.2:g.93725C= , LRG_567:g.93725C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000685801.1:c.3040-252C=	ENSP00000510688.1:n.3040-252C=
ENST00000691109.1:n.3272-252C=
ENST00000216181.11:c.2977-252C= MANE Select	ENSP00000216181.6:n.2977-252C=
ENST00000216181.9:c.2977-252C=	ENSP00000216181.5:n.2977-252C=
NM_002473.5:c.2977-252C= , LRG_567t1:c.2977-252C=	NP_002464.1:n.2977-252C=
XM_011530197.1:c.2977-252C=	XP_011528499.1:n.2977-252C=
XM_011530197.2:c.2977-252C=	XP_011528499.1:n.2977-252C=
XM_017028803.1:c.2977-252C=	XP_016884292.1:n.2977-252C=
XM_017028804.1:c.2977-252C=	XP_016884293.1:n.2977-252C=
XM_017028805.1:c.2977-252C=	XP_016884294.1:n.2977-252C=
XM_017028806.1:c.2977-252C=	XP_016884295.1:n.2977-252C=
NM_002473.6:c.2977-252C= MANE Select	NP_002464.1:n.2977-252C=