Canonical Allele Identifier: CA2656426383
Gene: MYH9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281983A>C , CM000684.2:g.36281983A>C GRCh38
NC_000022.10:g.36678029A>C , CM000684.1:g.36678029A>C GRCh37
NC_000022.9:g.35007975A>C NCBI36
NG_011884.2:g.111036T>G , LRG_567:g.111036T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.3001T>G
ENST00000685801.1:c.*685T>G ENSP00000510688.1:n.*685T>G
ENST00000690244.1:n.1904T>G
ENST00000691109.1:n.6863T>G
ENST00000216181.11:c.*685T>G MANE Select ENSP00000216181.6:n.*685T>G
ENST00000216181.9:c.*685T>G ENSP00000216181.5:n.*685T>G
NM_002473.5:c.*685T>G , LRG_567t1:c.*685T>G NP_002464.1:n.*685T>G
XM_011530197.1:c.*685T>G XP_011528499.1:n.*685T>G
XM_011530197.2:c.*685T>G XP_011528499.1:n.*685T>G
XM_017028803.1:c.*685T>G XP_016884292.1:n.*685T>G
XM_017028804.1:c.*685T>G XP_016884293.1:n.*685T>G
XM_017028805.1:c.*685T>G XP_016884294.1:n.*685T>G
XM_017028806.1:c.*685T>G XP_016884295.1:n.*685T>G
NM_002473.6:c.*685T>G MANE Select NP_002464.1:n.*685T>G