Canonical Allele Identifier: CA1770267690
Gene: HR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123636G= , CM000670.2:g.22123636G= GRCh38
NC_000008.10:g.21981149G= , CM000670.1:g.21981149G= GRCh37
NC_000008.9:g.22037094G= NCBI36
NG_008166.1:g.11882C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1915+13C= MANE Select ENSP00000370826.4:n.1915+13C=
ENST00000680789.1:c.1915+13C= ENSP00000505181.1:n.1915+13C=
ENST00000312841.9:c.1915+13C= ENSP00000326765.8:n.1915+13C=
ENST00000381418.8:c.1915+13C= ENSP00000370826.4:n.1915+13C=
NM_005144.4:c.1915+13C= NP_005135.2:n.1915+13C=
NM_018411.4:c.1915+13C= NP_060881.2:n.1915+13C=
XM_005273569.1:c.1918+13C= XP_005273626.1:n.1918+13C=
XM_006716367.1:c.1918+13C= XP_006716430.1:n.1918+13C=
XM_005273569.2:c.1918+13C= XP_005273626.1:n.1918+13C=
XM_006716367.2:c.1918+13C= XP_006716430.1:n.1918+13C=
NM_005144.5:c.1915+13C= MANE Select NP_005135.2:n.1915+13C=