Canonical Allele Identifier: CA323607129

Gene: MYH9

Linked Data

• dbSNP Id: rs545082607
• gnomAD v3: 22-36322403-A-T
• gnomAD v4: 22-36322403-A-T
• MyVariant Identifiers: chr22:g.36718448A>T (hg19) ; chr22:g.36322403A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36322403A>T , CM000684.2:g.36322403A>T	GRCh38
NC_000022.10:g.36718448A>T , CM000684.1:g.36718448A>T	GRCh37
NC_000022.9:g.35048394A>T	NCBI36
NG_011884.2:g.70616T>A , LRG_567:g.70616T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000685187.1:n.919+26T>A
ENST00000685191.1:n.928+26T>A
ENST00000685801.1:c.705+26T>A	ENSP00000510688.1:n.705+26T>A
ENST00000691109.1:n.566+26T>A
ENST00000691687.1:n.919+26T>A
ENST00000692930.1:n.919+26T>A
ENST00000216181.11:c.705+26T>A MANE Select	ENSP00000216181.6:n.705+26T>A
ENST00000216181.9:c.705+26T>A	ENSP00000216181.5:n.705+26T>A
ENST00000463027.1:n.309+26T>A
NM_002473.5:c.705+26T>A , LRG_567t1:c.705+26T>A	NP_002464.1:n.705+26T>A
XM_011530197.1:c.705+26T>A	XP_011528499.1:n.705+26T>A
XM_011530197.2:c.705+26T>A	XP_011528499.1:n.705+26T>A
XM_017028803.1:c.705+26T>A	XP_016884292.1:n.705+26T>A
XM_017028804.1:c.705+26T>A	XP_016884293.1:n.705+26T>A
XM_017028805.1:c.705+26T>A	XP_016884294.1:n.705+26T>A
XM_017028806.1:c.705+26T>A	XP_016884295.1:n.705+26T>A
NM_002473.6:c.705+26T>A MANE Select	NP_002464.1:n.705+26T>A