Canonical Allele Identifier: CA1024982674

Gene: HORMAD2

Linked Data

• dbSNP Id: rs2412980
• gnomAD v3: 22-30196080-T-A
• gnomAD v4: 22-30196080-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30196080T>A , CM000684.2:g.30196080T>A	GRCh38
NC_000022.10:g.30592069T>A , CM000684.1:g.30592069T>A	GRCh37
NC_000022.9:g.28922069T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_006724147.2:c.820-10905T>A	XP_006724210.2:n.820-10905T>A
XM_011529913.1:c.820-10905T>A	XP_011528215.1:n.820-10905T>A
XM_011529914.1:c.820-10905T>A	XP_011528216.1:n.820-10905T>A
XM_011529915.1:c.820-10905T>A	XP_011528217.1:n.820-10905T>A
XM_011529916.1:c.820-10905T>A	XP_011528218.1:n.820-10905T>A
XM_011529919.1:c.556-10905T>A	XP_011528221.1:n.556-10905T>A
XR_938153.1:n.88-3850A>T
XM_011529914.2:c.820-10905T>A	XP_011528216.1:n.820-10905T>A
XM_017028621.1:c.820-10905T>A	XP_016884110.1:n.820-10905T>A
XM_017028622.1:c.820-10905T>A	XP_016884111.1:n.820-10905T>A
XM_017028624.1:c.556-10905T>A	XP_016884113.1:n.556-10905T>A
XM_017028625.1:c.508-10905T>A	XP_016884114.1:n.508-10905T>A
XM_017028626.1:c.418-10905T>A	XP_016884115.1:n.418-10905T>A
XR_938153.3:n.151-3850A>T