Canonical Allele Identifier: CA2656426320
Gene: MYH9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36281924C>G , CM000684.2:g.36281924C>G GRCh38
NC_000022.10:g.36677970C>G , CM000684.1:g.36677970C>G GRCh37
NC_000022.9:g.35007916C>G NCBI36
NG_011884.2:g.111095G>C , LRG_567:g.111095G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000685708.1:n.3060G>C
ENST00000685801.1:c.*744G>C ENSP00000510688.1:n.*744G>C
ENST00000690244.1:n.1963G>C
ENST00000691109.1:n.6922G>C
ENST00000216181.11:c.*744G>C MANE Select ENSP00000216181.6:n.*744G>C
ENST00000216181.9:c.*744G>C ENSP00000216181.5:n.*744G>C
NM_002473.5:c.*744G>C , LRG_567t1:c.*744G>C NP_002464.1:n.*744G>C
XM_011530197.1:c.*744G>C XP_011528499.1:n.*744G>C
XM_011530197.2:c.*744G>C XP_011528499.1:n.*744G>C
XM_017028803.1:c.*744G>C XP_016884292.1:n.*744G>C
XM_017028804.1:c.*744G>C XP_016884293.1:n.*744G>C
XM_017028805.1:c.*744G>C XP_016884294.1:n.*744G>C
XM_017028806.1:c.*744G>C XP_016884295.1:n.*744G>C
NM_002473.6:c.*744G>C MANE Select NP_002464.1:n.*744G>C