Canonical Allele Identifier: CA411372852

Gene: MYH9

Linked Data

• gnomAD v4: 22-36284413-T-C
• MyVariant Identifiers: chr22:g.36680459T>C (hg19) ; chr22:g.36284413T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284413T>C , CM000684.2:g.36284413T>C	GRCh38
NC_000022.10:g.36680459T>C , CM000684.1:g.36680459T>C	GRCh37
NC_000022.9:g.35010405T>C	NCBI36
NG_011884.2:g.108606A>G , LRG_567:g.108606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2015A>G
ENST00000685801.1:c.5645A>G	ENSP00000510688.1:p.Tyr1882Cys
ENST00000690244.1:n.918A>G
ENST00000691109.1:n.5877A>G
ENST00000216181.11:c.5582A>G MANE Select	ENSP00000216181.6:p.Tyr1861Cys
ENST00000216181.9:c.5582A>G	ENSP00000216181.5:p.Tyr1861Cys
ENST00000475726.5:n.612A>G
ENST00000486218.1:n.589A>G
NM_002473.5:c.5582A>G , LRG_567t1:c.5582A>G	NP_002464.1:p.Tyr1861Cys
XM_011530197.1:c.5582A>G	XP_011528499.1:p.Tyr1861Cys
XM_011530197.2:c.5582A>G	XP_011528499.1:p.Tyr1861Cys
XM_017028803.1:c.5582A>G	XP_016884292.1:p.Tyr1861Cys
XM_017028804.1:c.5582A>G	XP_016884293.1:p.Tyr1861Cys
XM_017028805.1:c.5582A>G	XP_016884294.1:p.Tyr1861Cys
XM_017028806.1:c.5582A>G	XP_016884295.1:p.Tyr1861Cys
NM_002473.6:c.5582A>G MANE Select	NP_002464.1:p.Tyr1861Cys