Canonical Allele Identifier: CA370492570
Gene: HR HGNC NCBI

Linked Data

dbSNP Id: rs1332957009
gnomAD v2: 8-21981251-T-C
gnomAD v3: 8-22123738-T-C
gnomAD v4: 8-22123738-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123738T>C , CM000670.2:g.22123738T>C GRCh38
NC_000008.10:g.21981251T>C , CM000670.1:g.21981251T>C GRCh37
NC_000008.9:g.22037196T>C NCBI36
NG_008166.1:g.11780A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1826A>G MANE Select ENSP00000370826.4:p.Asn609Ser
ENST00000680789.1:c.1826A>G ENSP00000505181.1:p.Asn609Ser
ENST00000312841.9:c.1826A>G ENSP00000326765.8:p.Asn609Ser
ENST00000381418.8:c.1826A>G ENSP00000370826.4:p.Asn609Ser
NM_005144.4:c.1826A>G NP_005135.2:p.Asn609Ser
NM_018411.4:c.1826A>G NP_060881.2:p.Asn609Ser
XM_005273569.1:c.1829A>G XP_005273626.1:p.Asn610Ser
XM_006716367.1:c.1829A>G XP_006716430.1:p.Asn610Ser
XM_005273569.2:c.1829A>G XP_005273626.1:p.Asn610Ser
XM_006716367.2:c.1829A>G XP_006716430.1:p.Asn610Ser
NM_005144.5:c.1826A>G MANE Select NP_005135.2:p.Asn609Ser