Canonical Allele Identifier: CA2403799690
Gene: MYH9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36292131C= , CM000684.2:g.36292131C= GRCh38
NC_000022.10:g.36688177C= , CM000684.1:g.36688177C= GRCh37
NC_000022.9:g.35018123C= NCBI36
NG_011884.2:g.100888G= , LRG_567:g.100888G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000685801.1:c.4262G= ENSP00000510688.1:p.Arg1421=
ENST00000691109.1:n.4494G=
ENST00000216181.11:c.4199G= MANE Select ENSP00000216181.6:p.Arg1400=
ENST00000216181.9:c.4199G= ENSP00000216181.5:p.Arg1400=
NM_002473.5:c.4199G= , LRG_567t1:c.4199G= NP_002464.1:p.Arg1400=
XM_011530197.1:c.4199G= XP_011528499.1:p.Arg1400=
XM_011530197.2:c.4199G= XP_011528499.1:p.Arg1400=
XM_017028803.1:c.4199G= XP_016884292.1:p.Arg1400=
XM_017028804.1:c.4199G= XP_016884293.1:p.Arg1400=
XM_017028805.1:c.4199G= XP_016884294.1:p.Arg1400=
XM_017028806.1:c.4199G= XP_016884295.1:p.Arg1400=
NM_002473.6:c.4199G= MANE Select NP_002464.1:p.Arg1400=
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