Canonical Allele Identifier: CA2400915757
Gene: HORMAD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30196017A= , CM000684.2:g.30196017A= GRCh38
NC_000022.10:g.30592006A= , CM000684.1:g.30592006A= GRCh37
NC_000022.9:g.28922006A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006724147.2:c.820-10968A= XP_006724210.2:n.820-10968A=
XM_011529913.1:c.820-10968A= XP_011528215.1:n.820-10968A=
XM_011529914.1:c.820-10968A= XP_011528216.1:n.820-10968A=
XM_011529915.1:c.820-10968A= XP_011528217.1:n.820-10968A=
XM_011529916.1:c.820-10968A= XP_011528218.1:n.820-10968A=
XM_011529919.1:c.556-10968A= XP_011528221.1:n.556-10968A=
XR_938153.1:n.88-3787T=
XM_011529914.2:c.820-10968A= XP_011528216.1:n.820-10968A=
XM_017028621.1:c.820-10968A= XP_016884110.1:n.820-10968A=
XM_017028622.1:c.820-10968A= XP_016884111.1:n.820-10968A=
XM_017028624.1:c.556-10968A= XP_016884113.1:n.556-10968A=
XM_017028625.1:c.508-10968A= XP_016884114.1:n.508-10968A=
XM_017028626.1:c.418-10968A= XP_016884115.1:n.418-10968A=
XR_938153.3:n.151-3787T=