Canonical Allele Identifier: CA2656426634

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282174-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282174G>C , CM000684.2:g.36282174G>C	GRCh38
NC_000022.10:g.36678220G>C , CM000684.1:g.36678220G>C	GRCh37
NC_000022.9:g.35008166G>C	NCBI36
NG_011884.2:g.110845C>G , LRG_567:g.110845C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2810C>G
ENST00000685801.1:c.*494C>G	ENSP00000510688.1:n.*494C>G
ENST00000690244.1:n.1713C>G
ENST00000691109.1:n.6672C>G
ENST00000216181.11:c.*494C>G MANE Select	ENSP00000216181.6:n.*494C>G
ENST00000216181.9:c.*494C>G	ENSP00000216181.5:n.*494C>G
NM_002473.5:c.*494C>G , LRG_567t1:c.*494C>G	NP_002464.1:n.*494C>G
XM_011530197.1:c.*494C>G	XP_011528499.1:n.*494C>G
XM_011530197.2:c.*494C>G	XP_011528499.1:n.*494C>G
XM_017028803.1:c.*494C>G	XP_016884292.1:n.*494C>G
XM_017028804.1:c.*494C>G	XP_016884293.1:n.*494C>G
XM_017028805.1:c.*494C>G	XP_016884294.1:n.*494C>G
XM_017028806.1:c.*494C>G	XP_016884295.1:n.*494C>G
NM_002473.6:c.*494C>G MANE Select	NP_002464.1:n.*494C>G