Canonical Allele Identifier: CA4662447
Gene: HR HGNC NCBI

Linked Data

dbSNP Id: rs751712888
gnomAD v2: 8-21983174-T-C
gnomAD v3: 8-22125661-T-C
gnomAD v4: 8-22125661-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22125661T>C , CM000670.2:g.22125661T>C GRCh38
NC_000008.10:g.21983174T>C , CM000670.1:g.21983174T>C GRCh37
NC_000008.9:g.22039119T>C NCBI36
NG_008166.1:g.9857A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381418.9:c.1477A>G MANE Select ENSP00000370826.4:p.Lys493Glu
ENST00000680789.1:c.1477A>G ENSP00000505181.1:p.Lys493Glu
ENST00000312841.9:c.1477A>G ENSP00000326765.8:p.Lys493Glu
ENST00000381418.8:c.1477A>G ENSP00000370826.4:p.Lys493Glu
NM_005144.4:c.1477A>G NP_005135.2:p.Lys493Glu
NM_018411.4:c.1477A>G NP_060881.2:p.Lys493Glu
XM_005273569.1:c.1477A>G XP_005273626.1:p.Lys493Glu
XM_006716367.1:c.1477A>G XP_006716430.1:p.Lys493Glu
XM_005273569.2:c.1477A>G XP_005273626.1:p.Lys493Glu
XM_006716367.2:c.1477A>G XP_006716430.1:p.Lys493Glu
NM_005144.5:c.1477A>G MANE Select NP_005135.2:p.Lys493Glu