Canonical Allele Identifier: CA10627450

Gene: HR

Linked Data

• ClinVar Variation Id: 362463
• ClinVar RCV Id: RCV000322893 ; RCV000359229
• dbSNP Id: rs886062803
• gnomAD v4: 8-22115103-G-A
• MyVariant Identifiers: chr8:g.21972616G>A (hg19) ; chr8:g.22115103G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22115103G>A , CM000670.2:g.22115103G>A	GRCh38
NC_000008.10:g.21972616G>A , CM000670.1:g.21972616G>A	GRCh37
NC_000008.9:g.22028561G>A	NCBI36
NG_008166.1:g.20415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.*597C>T MANE Select	ENSP00000370826.4:n.*597C>T
ENST00000680789.1:c.*597C>T	ENSP00000505181.1:n.*597C>T
ENST00000312841.9:c.*597C>T	ENSP00000326765.8:n.*597C>T
ENST00000381418.8:c.*597C>T	ENSP00000370826.4:n.*597C>T
ENST00000522016.1:n.2360C>T
NM_005144.4:c.*597C>T	NP_005135.2:n.*597C>T
NM_018411.4:c.*597C>T	NP_060881.2:n.*597C>T
XM_005273569.1:c.*597C>T	XP_005273626.1:n.*597C>T
XM_006716367.1:c.*597C>T	XP_006716430.1:n.*597C>T
XM_005273569.2:c.*597C>T	XP_005273626.1:n.*597C>T
XM_006716367.2:c.*597C>T	XP_006716430.1:n.*597C>T
NM_005144.5:c.*597C>T MANE Select	NP_005135.2:n.*597C>T