Canonical Allele Identifier: CA370492530

Gene: HR

Linked Data

• gnomAD v4: 8-22123727-G-C
• MyVariant Identifiers: chr8:g.21981240G>C (hg19) ; chr8:g.22123727G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123727G>C , CM000670.2:g.22123727G>C	GRCh38
NC_000008.10:g.21981240G>C , CM000670.1:g.21981240G>C	GRCh37
NC_000008.9:g.22037185G>C	NCBI36
NG_008166.1:g.11791C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381418.9:c.1837C>G MANE Select	ENSP00000370826.4:p.Arg613Gly
ENST00000680789.1:c.1837C>G	ENSP00000505181.1:p.Arg613Gly
ENST00000312841.9:c.1837C>G	ENSP00000326765.8:p.Arg613Gly
ENST00000381418.8:c.1837C>G	ENSP00000370826.4:p.Arg613Gly
NM_005144.4:c.1837C>G	NP_005135.2:p.Arg613Gly
NM_018411.4:c.1837C>G	NP_060881.2:p.Arg613Gly
XM_005273569.1:c.1840C>G	XP_005273626.1:p.Arg614Gly
XM_006716367.1:c.1840C>G	XP_006716430.1:p.Arg614Gly
XM_005273569.2:c.1840C>G	XP_005273626.1:p.Arg614Gly
XM_006716367.2:c.1840C>G	XP_006716430.1:p.Arg614Gly
NM_005144.5:c.1837C>G MANE Select	NP_005135.2:p.Arg613Gly