Canonical Allele Identifier: CA2686428973

Gene: HR

Linked Data

• dbSNP Id: rs2131748767
• gnomAD v4: 8-22116481-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116481G>A , CM000670.2:g.22116481G>A	GRCh38
NC_000008.10:g.21973994G>A , CM000670.1:g.21973994G>A	GRCh37
NC_000008.9:g.22029939G>A	NCBI36
NG_008166.1:g.19037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-53C>T MANE Select	ENSP00000370826.4:n.3379-53C>T
ENST00000680789.1:c.3379-53C>T	ENSP00000505181.1:n.3379-53C>T
ENST00000312841.9:c.3214-53C>T	ENSP00000326765.8:n.3214-53C>T
ENST00000381418.8:c.3379-53C>T	ENSP00000370826.4:n.3379-53C>T
ENST00000522016.1:n.1572-53C>T
NM_005144.4:c.3379-53C>T	NP_005135.2:n.3379-53C>T
NM_018411.4:c.3214-53C>T	NP_060881.2:n.3214-53C>T
XM_005273569.1:c.3382-53C>T	XP_005273626.1:n.3382-53C>T
XM_006716367.1:c.3217-53C>T	XP_006716430.1:n.3217-53C>T
XM_005273569.2:c.3382-53C>T	XP_005273626.1:n.3382-53C>T
XM_006716367.2:c.3217-53C>T	XP_006716430.1:n.3217-53C>T
NM_005144.5:c.3379-53C>T MANE Select	NP_005135.2:n.3379-53C>T