Canonical Allele Identifier: CA370492551

Gene: HR

Linked Data

• gnomAD v4: 8-22123733-G-T
• MyVariant Identifiers: chr8:g.21981246G>T (hg19) ; chr8:g.22123733G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123733G>T , CM000670.2:g.22123733G>T	GRCh38
NC_000008.10:g.21981246G>T , CM000670.1:g.21981246G>T	GRCh37
NC_000008.9:g.22037191G>T	NCBI36
NG_008166.1:g.11785C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381418.9:c.1831C>A MANE Select	ENSP00000370826.4:p.His611Asn
ENST00000680789.1:c.1831C>A	ENSP00000505181.1:p.His611Asn
ENST00000312841.9:c.1831C>A	ENSP00000326765.8:p.His611Asn
ENST00000381418.8:c.1831C>A	ENSP00000370826.4:p.His611Asn
NM_005144.4:c.1831C>A	NP_005135.2:p.His611Asn
NM_018411.4:c.1831C>A	NP_060881.2:p.His611Asn
XM_005273569.1:c.1834C>A	XP_005273626.1:p.His612Asn
XM_006716367.1:c.1834C>A	XP_006716430.1:p.His612Asn
XM_005273569.2:c.1834C>A	XP_005273626.1:p.His612Asn
XM_006716367.2:c.1834C>A	XP_006716430.1:p.His612Asn
NM_005144.5:c.1831C>A MANE Select	NP_005135.2:p.His611Asn