Canonical Allele Identifier: CA2656428126

Gene: MYH9

Linked Data

• gnomAD v4: 22-36284363-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284363A>T , CM000684.2:g.36284363A>T	GRCh38
NC_000022.10:g.36680409A>T , CM000684.1:g.36680409A>T	GRCh37
NC_000022.9:g.35010355A>T	NCBI36
NG_011884.2:g.108656T>A , LRG_567:g.108656T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2025+40T>A
ENST00000685801.1:c.5655+40T>A	ENSP00000510688.1:n.5655+40T>A
ENST00000690244.1:n.928+40T>A
ENST00000691109.1:n.5887+40T>A
ENST00000216181.11:c.5592+40T>A MANE Select	ENSP00000216181.6:n.5592+40T>A
ENST00000216181.9:c.5592+40T>A	ENSP00000216181.5:n.5592+40T>A
ENST00000475726.5:n.622+40T>A
ENST00000486218.1:n.639T>A
NM_002473.5:c.5592+40T>A , LRG_567t1:c.5592+40T>A	NP_002464.1:n.5592+40T>A
XM_011530197.1:c.5592+40T>A	XP_011528499.1:n.5592+40T>A
XM_011530197.2:c.5592+40T>A	XP_011528499.1:n.5592+40T>A
XM_017028803.1:c.5592+40T>A	XP_016884292.1:n.5592+40T>A
XM_017028804.1:c.5592+40T>A	XP_016884293.1:n.5592+40T>A
XM_017028805.1:c.5592+40T>A	XP_016884294.1:n.5592+40T>A
XM_017028806.1:c.5592+40T>A	XP_016884295.1:n.5592+40T>A
NM_002473.6:c.5592+40T>A MANE Select	NP_002464.1:n.5592+40T>A