Canonical Allele Identifier: CA411372879

Gene: MYH9

Linked Data

• MyVariant Identifiers: chr22:g.36680471T>G (hg19) ; chr22:g.36284425T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284425T>G , CM000684.2:g.36284425T>G	GRCh38
NC_000022.10:g.36680471T>G , CM000684.1:g.36680471T>G	GRCh37
NC_000022.9:g.35010417T>G	NCBI36
NG_011884.2:g.108594A>C , LRG_567:g.108594A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2003A>C
ENST00000685801.1:c.5633A>C	ENSP00000510688.1:p.Asn1878Thr
ENST00000690244.1:n.906A>C
ENST00000691109.1:n.5865A>C
ENST00000216181.11:c.5570A>C MANE Select	ENSP00000216181.6:p.Asn1857Thr
ENST00000216181.9:c.5570A>C	ENSP00000216181.5:p.Asn1857Thr
ENST00000475726.5:n.600A>C
ENST00000486218.1:n.577A>C
NM_002473.5:c.5570A>C , LRG_567t1:c.5570A>C	NP_002464.1:p.Asn1857Thr
XM_011530197.1:c.5570A>C	XP_011528499.1:p.Asn1857Thr
XM_011530197.2:c.5570A>C	XP_011528499.1:p.Asn1857Thr
XM_017028803.1:c.5570A>C	XP_016884292.1:p.Asn1857Thr
XM_017028804.1:c.5570A>C	XP_016884293.1:p.Asn1857Thr
XM_017028805.1:c.5570A>C	XP_016884294.1:p.Asn1857Thr
XM_017028806.1:c.5570A>C	XP_016884295.1:p.Asn1857Thr
NM_002473.6:c.5570A>C MANE Select	NP_002464.1:p.Asn1857Thr