Canonical Allele Identifier: CA1024982685

Gene: HORMAD2

Linked Data

• dbSNP Id: rs1927424918
• gnomAD v3: 22-30196119-A-G
• gnomAD v4: 22-30196119-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30196119A>G , CM000684.2:g.30196119A>G	GRCh38
NC_000022.10:g.30592108A>G , CM000684.1:g.30592108A>G	GRCh37
NC_000022.9:g.28922108A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_006724147.2:c.820-10866A>G	XP_006724210.2:n.820-10866A>G
XM_011529913.1:c.820-10866A>G	XP_011528215.1:n.820-10866A>G
XM_011529914.1:c.820-10866A>G	XP_011528216.1:n.820-10866A>G
XM_011529915.1:c.820-10866A>G	XP_011528217.1:n.820-10866A>G
XM_011529916.1:c.820-10866A>G	XP_011528218.1:n.820-10866A>G
XM_011529919.1:c.556-10866A>G	XP_011528221.1:n.556-10866A>G
XR_938153.1:n.88-3889T>C
XM_011529914.2:c.820-10866A>G	XP_011528216.1:n.820-10866A>G
XM_017028621.1:c.820-10866A>G	XP_016884110.1:n.820-10866A>G
XM_017028622.1:c.820-10866A>G	XP_016884111.1:n.820-10866A>G
XM_017028624.1:c.556-10866A>G	XP_016884113.1:n.556-10866A>G
XM_017028625.1:c.508-10866A>G	XP_016884114.1:n.508-10866A>G
XM_017028626.1:c.418-10866A>G	XP_016884115.1:n.418-10866A>G
XR_938153.3:n.151-3889T>C