Canonical Allele Identifier: CA459904776

Gene: HR

Linked Data

• MyVariant Identifiers: chr8:g.21973885G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116372G>C , CM000670.2:g.22116372G>C	GRCh38
NC_000008.10:g.21973885G>C , CM000670.1:g.21973885G>C	GRCh37
NC_000008.9:g.22029830G>C	NCBI36
NG_008166.1:g.19146C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3435C>G MANE Select	ENSP00000370826.4:p.Thr1145=
ENST00000680789.1:c.3435C>G	ENSP00000505181.1:p.Thr1145=
ENST00000312841.9:c.3270C>G	ENSP00000326765.8:p.Thr1090=
ENST00000381418.8:c.3435C>G	ENSP00000370826.4:p.Thr1145=
ENST00000522016.1:n.1628C>G
NM_005144.4:c.3435C>G	NP_005135.2:p.Thr1145=
NM_018411.4:c.3270C>G	NP_060881.2:p.Thr1090=
XM_005273569.1:c.3438C>G	XP_005273626.1:p.Thr1146=
XM_006716367.1:c.3273C>G	XP_006716430.1:p.Thr1091=
XM_005273569.2:c.3438C>G	XP_005273626.1:p.Thr1146=
XM_006716367.2:c.3273C>G	XP_006716430.1:p.Thr1091=
NM_005144.5:c.3435C>G MANE Select	NP_005135.2:p.Thr1145=