Canonical Allele Identifier: CA514351325

Gene: MYH9

Linked Data

• dbSNP Id: rs80338835
• gnomAD v3: 22-36282754-G-T
• gnomAD v4: 22-36282754-G-T
• MyVariant Identifiers: chr22:g.36678800G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282754G>T , CM000684.2:g.36282754G>T	GRCh38
NC_000022.10:g.36678800G>T , CM000684.1:g.36678800G>T	GRCh37
NC_000022.9:g.35008746G>T	NCBI36
NG_011884.2:g.110265C>A , LRG_567:g.110265C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000685708.1:n.2230C>A
ENST00000685801.1:c.5860C>A	ENSP00000510688.1:p.Arg1954=
ENST00000690244.1:n.1133C>A
ENST00000691109.1:n.6092C>A
ENST00000216181.11:c.5797C>A MANE Select	ENSP00000216181.6:p.Arg1933=
ENST00000216181.9:c.5797C>A	ENSP00000216181.5:p.Arg1933=
NM_002473.5:c.5797C>A , LRG_567t1:c.5797C>A	NP_002464.1:p.Arg1933=
XM_011530197.1:c.5797C>A	XP_011528499.1:p.Arg1933=
XM_011530197.2:c.5797C>A	XP_011528499.1:p.Arg1933=
XM_017028803.1:c.5797C>A	XP_016884292.1:p.Arg1933=
XM_017028804.1:c.5797C>A	XP_016884293.1:p.Arg1933=
XM_017028805.1:c.5797C>A	XP_016884294.1:p.Arg1933=
XM_017028806.1:c.5797C>A	XP_016884295.1:p.Arg1933=
NM_002473.6:c.5797C>A MANE Select	NP_002464.1:p.Arg1933=