Canonical Allele Identifier: CA639151632

Gene: MYH9

Linked Data

• dbSNP Id: rs1222412087
• gnomAD v2: 22-36695244-TTTGAA-T
• gnomAD v3: 22-36299198-TTTGAA-T
• gnomAD v4: 22-36299198-TTTGAA-T
• MyVariant Identifiers: chr22:g.36695245_36695249del (hg19) ; chr22:g.36299199_36299203del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36299199_36299203del , CM000684.2:g.36299199_36299203del	GRCh38
NC_000022.10:g.36695245_36695249del , CM000684.1:g.36695245_36695249del	GRCh37
NC_000022.9:g.35025191_35025195del	NCBI36
NG_011884.2:g.93816_93820del , LRG_567:g.93816_93820del

Transcript Alleles

HGVS	Amino-acid change
ENST00000685801.1:c.3040-161_3040-157del	ENSP00000510688.1:n.3040-161_3040-157del
ENST00000691109.1:n.3272-161_3272-157del
ENST00000216181.11:c.2977-161_2977-157del MANE Select	ENSP00000216181.6:n.2977-161_2977-157del
ENST00000216181.9:c.2977-161_2977-157del	ENSP00000216181.5:n.2977-161_2977-157del
NM_002473.5:c.2977-161_2977-157del , LRG_567t1:c.2977-161_2977-157del	NP_002464.1:n.2977-161_2977-157del
XM_011530197.1:c.2977-161_2977-157del	XP_011528499.1:n.2977-161_2977-157del
XM_011530197.2:c.2977-161_2977-157del	XP_011528499.1:n.2977-161_2977-157del
XM_017028803.1:c.2977-161_2977-157del	XP_016884292.1:n.2977-161_2977-157del
XM_017028804.1:c.2977-161_2977-157del	XP_016884293.1:n.2977-161_2977-157del
XM_017028805.1:c.2977-161_2977-157del	XP_016884294.1:n.2977-161_2977-157del
XM_017028806.1:c.2977-161_2977-157del	XP_016884295.1:n.2977-161_2977-157del
NM_002473.6:c.2977-161_2977-157del MANE Select	NP_002464.1:n.2977-161_2977-157del