Canonical Allele Identifier: CA411372873

Gene: MYH9

Linked Data

• MyVariant Identifiers: chr22:g.36680468G>C (hg19) ; chr22:g.36284422G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284422G>C , CM000684.2:g.36284422G>C	GRCh38
NC_000022.10:g.36680468G>C , CM000684.1:g.36680468G>C	GRCh37
NC_000022.9:g.35010414G>C	NCBI36
NG_011884.2:g.108597C>G , LRG_567:g.108597C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2006C>G
ENST00000685801.1:c.5636C>G	ENSP00000510688.1:p.Ala1879Gly
ENST00000690244.1:n.909C>G
ENST00000691109.1:n.5868C>G
ENST00000216181.11:c.5573C>G MANE Select	ENSP00000216181.6:p.Ala1858Gly
ENST00000216181.9:c.5573C>G	ENSP00000216181.5:p.Ala1858Gly
ENST00000475726.5:n.603C>G
ENST00000486218.1:n.580C>G
NM_002473.5:c.5573C>G , LRG_567t1:c.5573C>G	NP_002464.1:p.Ala1858Gly
XM_011530197.1:c.5573C>G	XP_011528499.1:p.Ala1858Gly
XM_011530197.2:c.5573C>G	XP_011528499.1:p.Ala1858Gly
XM_017028803.1:c.5573C>G	XP_016884292.1:p.Ala1858Gly
XM_017028804.1:c.5573C>G	XP_016884293.1:p.Ala1858Gly
XM_017028805.1:c.5573C>G	XP_016884294.1:p.Ala1858Gly
XM_017028806.1:c.5573C>G	XP_016884295.1:p.Ala1858Gly
NM_002473.6:c.5573C>G MANE Select	NP_002464.1:p.Ala1858Gly