Canonical Allele Identifier: CA2528922957

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36322401A>G , CM000684.2:g.36322401A>G	GRCh38
NC_000022.10:g.36718446A>G , CM000684.1:g.36718446A>G	GRCh37
NC_000022.9:g.35048392A>G	NCBI36
NG_011884.2:g.70618T>C , LRG_567:g.70618T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000685187.1:n.919+28T>C
ENST00000685191.1:n.928+28T>C
ENST00000685801.1:c.705+28T>C	ENSP00000510688.1:n.705+28T>C
ENST00000691109.1:n.566+28T>C
ENST00000691687.1:n.919+28T>C
ENST00000692930.1:n.919+28T>C
ENST00000216181.11:c.705+28T>C MANE Select	ENSP00000216181.6:n.705+28T>C
ENST00000216181.9:c.705+28T>C	ENSP00000216181.5:n.705+28T>C
ENST00000463027.1:n.309+28T>C
NM_002473.5:c.705+28T>C , LRG_567t1:c.705+28T>C	NP_002464.1:n.705+28T>C
XM_011530197.1:c.705+28T>C	XP_011528499.1:n.705+28T>C
XM_011530197.2:c.705+28T>C	XP_011528499.1:n.705+28T>C
XM_017028803.1:c.705+28T>C	XP_016884292.1:n.705+28T>C
XM_017028804.1:c.705+28T>C	XP_016884293.1:n.705+28T>C
XM_017028805.1:c.705+28T>C	XP_016884294.1:n.705+28T>C
XM_017028806.1:c.705+28T>C	XP_016884295.1:n.705+28T>C
NM_002473.6:c.705+28T>C MANE Select	NP_002464.1:n.705+28T>C