Canonical Allele Identifier: CA2656428142

Gene: MYH9

Linked Data

• gnomAD v4: 22-36284389-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284389A>T , CM000684.2:g.36284389A>T	GRCh38
NC_000022.10:g.36680435A>T , CM000684.1:g.36680435A>T	GRCh37
NC_000022.9:g.35010381A>T	NCBI36
NG_011884.2:g.108630T>A , LRG_567:g.108630T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2025+14T>A
ENST00000685801.1:c.5655+14T>A	ENSP00000510688.1:n.5655+14T>A
ENST00000690244.1:n.928+14T>A
ENST00000691109.1:n.5887+14T>A
ENST00000216181.11:c.5592+14T>A MANE Select	ENSP00000216181.6:n.5592+14T>A
ENST00000216181.9:c.5592+14T>A	ENSP00000216181.5:n.5592+14T>A
ENST00000475726.5:n.622+14T>A
ENST00000486218.1:n.613T>A
NM_002473.5:c.5592+14T>A , LRG_567t1:c.5592+14T>A	NP_002464.1:n.5592+14T>A
XM_011530197.1:c.5592+14T>A	XP_011528499.1:n.5592+14T>A
XM_011530197.2:c.5592+14T>A	XP_011528499.1:n.5592+14T>A
XM_017028803.1:c.5592+14T>A	XP_016884292.1:n.5592+14T>A
XM_017028804.1:c.5592+14T>A	XP_016884293.1:n.5592+14T>A
XM_017028805.1:c.5592+14T>A	XP_016884294.1:n.5592+14T>A
XM_017028806.1:c.5592+14T>A	XP_016884295.1:n.5592+14T>A
NM_002473.6:c.5592+14T>A MANE Select	NP_002464.1:n.5592+14T>A