Canonical Allele Identifier: CA370513689

Gene: HR

Linked Data

• MyVariant Identifiers: chr8:g.21973817G>C (hg19) ; chr8:g.22116304G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116304G>C , CM000670.2:g.22116304G>C	GRCh38
NC_000008.10:g.21973817G>C , CM000670.1:g.21973817G>C	GRCh37
NC_000008.9:g.22029762G>C	NCBI36
NG_008166.1:g.19214C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3503C>G MANE Select	ENSP00000370826.4:p.Ala1168Gly
ENST00000680789.1:c.3503C>G	ENSP00000505181.1:p.Ala1168Gly
ENST00000312841.9:c.3338C>G	ENSP00000326765.8:p.Ala1113Gly
ENST00000381418.8:c.3503C>G	ENSP00000370826.4:p.Ala1168Gly
ENST00000522016.1:n.1696C>G
NM_005144.4:c.3503C>G	NP_005135.2:p.Ala1168Gly
NM_018411.4:c.3338C>G	NP_060881.2:p.Ala1113Gly
XM_005273569.1:c.3506C>G	XP_005273626.1:p.Ala1169Gly
XM_006716367.1:c.3341C>G	XP_006716430.1:p.Ala1114Gly
XM_005273569.2:c.3506C>G	XP_005273626.1:p.Ala1169Gly
XM_006716367.2:c.3341C>G	XP_006716430.1:p.Ala1114Gly
NM_005144.5:c.3503C>G MANE Select	NP_005135.2:p.Ala1168Gly