Canonical Allele Identifier: CA2686436785
Gene: HR HGNC NCBI

Linked Data

gnomAD v4: 8-22123637-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123637C>A , CM000670.2:g.22123637C>A GRCh38
NC_000008.10:g.21981150C>A , CM000670.1:g.21981150C>A GRCh37
NC_000008.9:g.22037095C>A NCBI36
NG_008166.1:g.11881G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1915+12G>T MANE Select ENSP00000370826.4:n.1915+12G>T
ENST00000680789.1:c.1915+12G>T ENSP00000505181.1:n.1915+12G>T
ENST00000312841.9:c.1915+12G>T ENSP00000326765.8:n.1915+12G>T
ENST00000381418.8:c.1915+12G>T ENSP00000370826.4:n.1915+12G>T
NM_005144.4:c.1915+12G>T NP_005135.2:n.1915+12G>T
NM_018411.4:c.1915+12G>T NP_060881.2:n.1915+12G>T
XM_005273569.1:c.1918+12G>T XP_005273626.1:n.1918+12G>T
XM_006716367.1:c.1918+12G>T XP_006716430.1:n.1918+12G>T
XM_005273569.2:c.1918+12G>T XP_005273626.1:n.1918+12G>T
XM_006716367.2:c.1918+12G>T XP_006716430.1:n.1918+12G>T
NM_005144.5:c.1915+12G>T MANE Select NP_005135.2:n.1915+12G>T