Canonical Allele Identifier: CA370492615

Gene: HR

Linked Data

• gnomAD v4: 8-22123747-C-A
• MyVariant Identifiers: chr8:g.21981260C>A (hg19) ; chr8:g.22123747C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123747C>A , CM000670.2:g.22123747C>A	GRCh38
NC_000008.10:g.21981260C>A , CM000670.1:g.21981260C>A	GRCh37
NC_000008.9:g.22037205C>A	NCBI36
NG_008166.1:g.11771G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381418.9:c.1817G>T MANE Select	ENSP00000370826.4:p.Gly606Val
ENST00000680789.1:c.1817G>T	ENSP00000505181.1:p.Gly606Val
ENST00000312841.9:c.1817G>T	ENSP00000326765.8:p.Gly606Val
ENST00000381418.8:c.1817G>T	ENSP00000370826.4:p.Gly606Val
NM_005144.4:c.1817G>T	NP_005135.2:p.Gly606Val
NM_018411.4:c.1817G>T	NP_060881.2:p.Gly606Val
XM_005273569.1:c.1820G>T	XP_005273626.1:p.Gly607Val
XM_006716367.1:c.1820G>T	XP_006716430.1:p.Gly607Val
XM_005273569.2:c.1820G>T	XP_005273626.1:p.Gly607Val
XM_006716367.2:c.1820G>T	XP_006716430.1:p.Gly607Val
NM_005144.5:c.1817G>T MANE Select	NP_005135.2:p.Gly606Val