Canonical Allele Identifier: CA134522

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36298908C>G , CM000684.2:g.36298908C>G	GRCh38
NC_000022.10:g.36694954C>G , CM000684.1:g.36694954C>G	GRCh37
NC_000022.9:g.35024900C>G	NCBI36
NG_011884.2:g.94111G>C , LRG_567:g.94111G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685801.1:c.3163+11G>C	ENSP00000510688.1:n.3163+11G>C
ENST00000691109.1:n.3395+11G>C
ENST00000216181.11:c.3100+11G>C MANE Select	ENSP00000216181.6:n.3100+11G>C
ENST00000216181.9:c.3100+11G>C	ENSP00000216181.5:n.3100+11G>C
NM_002473.5:c.3100+11G>C , LRG_567t1:c.3100+11G>C	NP_002464.1:n.3100+11G>C
XM_011530197.1:c.3100+11G>C	XP_011528499.1:n.3100+11G>C
XM_011530197.2:c.3100+11G>C	XP_011528499.1:n.3100+11G>C
XM_017028803.1:c.3100+11G>C	XP_016884292.1:n.3100+11G>C
XM_017028804.1:c.3100+11G>C	XP_016884293.1:n.3100+11G>C
XM_017028805.1:c.3100+11G>C	XP_016884294.1:n.3100+11G>C
XM_017028806.1:c.3100+11G>C	XP_016884295.1:n.3100+11G>C
NM_002473.6:c.3100+11G>C MANE Select	NP_002464.1:n.3100+11G>C