Canonical Allele Identifier: CA752843528

Gene: MYH9

Linked Data

• dbSNP Id: rs1211659543
• MyVariant Identifiers: chr22:g.36751148G>C (hg19) ; chr22:g.36355103G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36355103G>C , CM000684.2:g.36355103G>C	GRCh38
NC_000022.10:g.36751148G>C , CM000684.1:g.36751148G>C	GRCh37
NC_000022.9:g.35081094G>C	NCBI36
NG_011884.2:g.37916C>G , LRG_567:g.37916C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000685187.1:n.196-5848C>G
ENST00000685191.1:n.205-5848C>G
ENST00000685801.1:c.-19-5848C>G	ENSP00000510688.1:n.-19-5848C>G
ENST00000688137.1:c.-19-5848C>G	ENSP00000510189.1:n.-19-5848C>G
ENST00000691296.1:c.-19-5848C>G	ENSP00000509816.1:n.-19-5848C>G
ENST00000691687.1:n.196-5848C>G
ENST00000692930.1:n.196-5848C>G
ENST00000216181.11:c.-19-5848C>G MANE Select	ENSP00000216181.6:n.-19-5848C>G
ENST00000216181.9:c.-19-5848C>G	ENSP00000216181.5:n.-19-5848C>G
ENST00000401701.1:c.-19-5848C>G	ENSP00000384631.1:n.-19-5848C>G
ENST00000456729.1:c.-19-5848C>G	ENSP00000414852.1:n.-19-5848C>G
NM_002473.5:c.-19-5848C>G , LRG_567t1:c.-19-5848C>G	NP_002464.1:n.-19-5848C>G
XM_011530197.1:c.-19-5848C>G	XP_011528499.1:n.-19-5848C>G
XM_011530197.2:c.-19-5848C>G	XP_011528499.1:n.-19-5848C>G
XM_017028803.1:c.-19-5848C>G	XP_016884292.1:n.-19-5848C>G
XM_017028804.1:c.-19-5848C>G	XP_016884293.1:n.-19-5848C>G
XM_017028806.1:c.-19-5848C>G	XP_016884295.1:n.-19-5848C>G
NM_002473.6:c.-19-5848C>G MANE Select	NP_002464.1:n.-19-5848C>G