Canonical Allele Identifier: CA10208938

Gene: MYH9

Linked Data

• ClinVar Variation Id: 2890483
• ClinVar RCV Id: RCV003720509
• dbSNP Id: rs766826415
• ExAC: 22:36680131 C / T
• gnomAD v2: 22-36680131-C-T
• gnomAD v3: 22-36284085-C-T
• gnomAD v4: 22-36284085-C-T
• MyVariant Identifiers: chr22:g.36680131C>T (hg19) ; chr22:g.36284085C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284085C>T , CM000684.2:g.36284085C>T	GRCh38
NC_000022.10:g.36680131C>T , CM000684.1:g.36680131C>T	GRCh37
NC_000022.9:g.35010077C>T	NCBI36
NG_011884.2:g.108934G>A , LRG_567:g.108934G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2198+8G>A
ENST00000685801.1:c.5828+8G>A	ENSP00000510688.1:n.5828+8G>A
ENST00000690244.1:n.1101+8G>A
ENST00000691109.1:n.6060+8G>A
ENST00000216181.11:c.5765+8G>A MANE Select	ENSP00000216181.6:n.5765+8G>A
ENST00000216181.9:c.5765+8G>A	ENSP00000216181.5:n.5765+8G>A
NM_002473.5:c.5765+8G>A , LRG_567t1:c.5765+8G>A	NP_002464.1:n.5765+8G>A
XM_011530197.1:c.5765+8G>A	XP_011528499.1:n.5765+8G>A
XM_011530197.2:c.5765+8G>A	XP_011528499.1:n.5765+8G>A
XM_017028803.1:c.5765+8G>A	XP_016884292.1:n.5765+8G>A
XM_017028804.1:c.5765+8G>A	XP_016884293.1:n.5765+8G>A
XM_017028805.1:c.5765+8G>A	XP_016884294.1:n.5765+8G>A
XM_017028806.1:c.5765+8G>A	XP_016884295.1:n.5765+8G>A
NM_002473.6:c.5765+8G>A MANE Select	NP_002464.1:n.5765+8G>A