Canonical Allele Identifier: CA370514194

Gene: HR

Linked Data

• MyVariant Identifiers: chr8:g.21973935C>G (hg19) ; chr8:g.22116422C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116422C>G , CM000670.2:g.22116422C>G	GRCh38
NC_000008.10:g.21973935C>G , CM000670.1:g.21973935C>G	GRCh37
NC_000008.9:g.22029880C>G	NCBI36
NG_008166.1:g.19096G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3385G>C MANE Select	ENSP00000370826.4:p.Gly1129Arg
ENST00000680789.1:c.3385G>C	ENSP00000505181.1:p.Gly1129Arg
ENST00000312841.9:c.3220G>C	ENSP00000326765.8:p.Gly1074Arg
ENST00000381418.8:c.3385G>C	ENSP00000370826.4:p.Gly1129Arg
ENST00000522016.1:n.1578G>C
NM_005144.4:c.3385G>C	NP_005135.2:p.Gly1129Arg
NM_018411.4:c.3220G>C	NP_060881.2:p.Gly1074Arg
XM_005273569.1:c.3388G>C	XP_005273626.1:p.Gly1130Arg
XM_006716367.1:c.3223G>C	XP_006716430.1:p.Gly1075Arg
XM_005273569.2:c.3388G>C	XP_005273626.1:p.Gly1130Arg
XM_006716367.2:c.3223G>C	XP_006716430.1:p.Gly1075Arg
NM_005144.5:c.3385G>C MANE Select	NP_005135.2:p.Gly1129Arg