Canonical Allele Identifier: CA2403803466
Gene: MYH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36299227G= , CM000684.2:g.36299227G= GRCh38
NC_000022.10:g.36695273G= , CM000684.1:g.36695273G= GRCh37
NC_000022.9:g.35025219G= NCBI36
NG_011884.2:g.93792C= , LRG_567:g.93792C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000685801.1:c.3040-185C= ENSP00000510688.1:n.3040-185C=
ENST00000691109.1:n.3272-185C=
ENST00000216181.11:c.2977-185C= MANE Select ENSP00000216181.6:n.2977-185C=
ENST00000216181.9:c.2977-185C= ENSP00000216181.5:n.2977-185C=
NM_002473.5:c.2977-185C= , LRG_567t1:c.2977-185C= NP_002464.1:n.2977-185C=
XM_011530197.1:c.2977-185C= XP_011528499.1:n.2977-185C=
XM_011530197.2:c.2977-185C= XP_011528499.1:n.2977-185C=
XM_017028803.1:c.2977-185C= XP_016884292.1:n.2977-185C=
XM_017028804.1:c.2977-185C= XP_016884293.1:n.2977-185C=
XM_017028805.1:c.2977-185C= XP_016884294.1:n.2977-185C=
XM_017028806.1:c.2977-185C= XP_016884295.1:n.2977-185C=
NM_002473.6:c.2977-185C= MANE Select NP_002464.1:n.2977-185C=