Canonical Allele Identifier: CA10651245
Gene: MYH9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 341471
dbSNP Id: rs12107

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281936G>A , CM000684.2:g.36281936G>A GRCh38
NC_000022.10:g.36677982G>A , CM000684.1:g.36677982G>A GRCh37
NC_000022.9:g.35007928G>A NCBI36
NG_011884.2:g.111083C>T , LRG_567:g.111083C>T

Transcript Alleles

HGVS Amino-acid change
NM_002473.5:c.*732C>T , LRG_567t1:c.*732C>T NP_002464.1:p.=
XM_011530197.1:c.*732C>T XP_011528499.1:p.=
XM_011530197.2:c.*732C>T
XM_017028803.1:c.*732C>T XP_016884292.1:p.=
XM_017028804.1:c.*732C>T XP_016884293.1:p.=
XM_017028805.1:c.*732C>T XP_016884294.1:p.=
XM_017028806.1:c.*732C>T XP_016884295.1:p.=
ENST00000216181.9:c.*732C>T ENSP00000216181.5:p.=