Canonical Allele Identifier: CA639392697

Gene: MYH9

Linked Data

• dbSNP Id: rs1271420364
• gnomAD v2: 22-36712725-C-T
• MyVariant Identifiers: chr22:g.36712725C>T (hg19) ; chr22:g.36316680C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316680C>T , CM000684.2:g.36316680C>T	GRCh38
NC_000022.10:g.36712725C>T , CM000684.1:g.36712725C>T	GRCh37
NC_000022.9:g.35042671C>T	NCBI36
NG_011884.2:g.76339G>A , LRG_567:g.76339G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1442-11G>A
ENST00000685801.1:c.1228-11G>A	ENSP00000510688.1:n.1228-11G>A
ENST00000691109.1:n.1523-11G>A
ENST00000691687.1:n.2026-11G>A
ENST00000692930.1:n.1442-11G>A
ENST00000216181.11:c.1228-11G>A MANE Select	ENSP00000216181.6:n.1228-11G>A
ENST00000216181.9:c.1228-11G>A	ENSP00000216181.5:n.1228-11G>A
ENST00000477189.1:n.416-11G>A
NM_002473.5:c.1228-11G>A , LRG_567t1:c.1228-11G>A	NP_002464.1:n.1228-11G>A
XM_011530197.1:c.1228-11G>A	XP_011528499.1:n.1228-11G>A
XM_011530197.2:c.1228-11G>A	XP_011528499.1:n.1228-11G>A
XM_017028803.1:c.1228-11G>A	XP_016884292.1:n.1228-11G>A
XM_017028804.1:c.1228-11G>A	XP_016884293.1:n.1228-11G>A
XM_017028805.1:c.1228-11G>A	XP_016884294.1:n.1228-11G>A
XM_017028806.1:c.1228-11G>A	XP_016884295.1:n.1228-11G>A
NM_002473.6:c.1228-11G>A MANE Select	NP_002464.1:n.1228-11G>A