Canonical Allele Identifier: CA411372860

Gene: MYH9

Linked Data

• MyVariant Identifiers: chr22:g.36680462T>A (hg19) ; chr22:g.36284416T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284416T>A , CM000684.2:g.36284416T>A	GRCh38
NC_000022.10:g.36680462T>A , CM000684.1:g.36680462T>A	GRCh37
NC_000022.9:g.35010408T>A	NCBI36
NG_011884.2:g.108603A>T , LRG_567:g.108603A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2012A>T
ENST00000685801.1:c.5642A>T	ENSP00000510688.1:p.Gln1881Leu
ENST00000690244.1:n.915A>T
ENST00000691109.1:n.5874A>T
ENST00000216181.11:c.5579A>T MANE Select	ENSP00000216181.6:p.Gln1860Leu
ENST00000216181.9:c.5579A>T	ENSP00000216181.5:p.Gln1860Leu
ENST00000475726.5:n.609A>T
ENST00000486218.1:n.586A>T
NM_002473.5:c.5579A>T , LRG_567t1:c.5579A>T	NP_002464.1:p.Gln1860Leu
XM_011530197.1:c.5579A>T	XP_011528499.1:p.Gln1860Leu
XM_011530197.2:c.5579A>T	XP_011528499.1:p.Gln1860Leu
XM_017028803.1:c.5579A>T	XP_016884292.1:p.Gln1860Leu
XM_017028804.1:c.5579A>T	XP_016884293.1:p.Gln1860Leu
XM_017028805.1:c.5579A>T	XP_016884294.1:p.Gln1860Leu
XM_017028806.1:c.5579A>T	XP_016884295.1:p.Gln1860Leu
NM_002473.6:c.5579A>T MANE Select	NP_002464.1:p.Gln1860Leu