Canonical Allele Identifier: CA2403794894
Gene: MYH9 HGNC NCBI

Linked Data

dbSNP Id: rs2016495372

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281893G>A , CM000684.2:g.36281893G>A GRCh38
NC_000022.10:g.36677939G>A , CM000684.1:g.36677939G>A GRCh37
NC_000022.9:g.35007885G>A NCBI36
NG_011884.2:g.111126C>T , LRG_567:g.111126C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.3091C>T
ENST00000685801.1:c.*775C>T ENSP00000510688.1:n.*775C>T
ENST00000690244.1:n.1994C>T
ENST00000691109.1:n.6953C>T
ENST00000216181.11:c.*775C>T MANE Select ENSP00000216181.6:n.*775C>T
ENST00000216181.9:c.*775C>T ENSP00000216181.5:n.*775C>T
NM_002473.5:c.*775C>T , LRG_567t1:c.*775C>T NP_002464.1:n.*775C>T
XM_011530197.1:c.*775C>T XP_011528499.1:n.*775C>T
XM_011530197.2:c.*775C>T XP_011528499.1:n.*775C>T
XM_017028803.1:c.*775C>T XP_016884292.1:n.*775C>T
XM_017028804.1:c.*775C>T XP_016884293.1:n.*775C>T
XM_017028805.1:c.*775C>T XP_016884294.1:n.*775C>T
XM_017028806.1:c.*775C>T XP_016884295.1:n.*775C>T
NM_002473.6:c.*775C>T MANE Select NP_002464.1:n.*775C>T