Canonical Allele Identifier: CA370513847

Gene: HR

Linked Data

• gnomAD v4: 8-22116340-C-A
• MyVariant Identifiers: chr8:g.21973853C>A (hg19) ; chr8:g.22116340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116340C>A , CM000670.2:g.22116340C>A	GRCh38
NC_000008.10:g.21973853C>A , CM000670.1:g.21973853C>A	GRCh37
NC_000008.9:g.22029798C>A	NCBI36
NG_008166.1:g.19178G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3467G>T MANE Select	ENSP00000370826.4:p.Gly1156Val
ENST00000680789.1:c.3467G>T	ENSP00000505181.1:p.Gly1156Val
ENST00000312841.9:c.3302G>T	ENSP00000326765.8:p.Gly1101Val
ENST00000381418.8:c.3467G>T	ENSP00000370826.4:p.Gly1156Val
ENST00000522016.1:n.1660G>T
NM_005144.4:c.3467G>T	NP_005135.2:p.Gly1156Val
NM_018411.4:c.3302G>T	NP_060881.2:p.Gly1101Val
XM_005273569.1:c.3470G>T	XP_005273626.1:p.Gly1157Val
XM_006716367.1:c.3305G>T	XP_006716430.1:p.Gly1102Val
XM_005273569.2:c.3470G>T	XP_005273626.1:p.Gly1157Val
XM_006716367.2:c.3305G>T	XP_006716430.1:p.Gly1102Val
NM_005144.5:c.3467G>T MANE Select	NP_005135.2:p.Gly1156Val