Canonical Allele Identifier: CA2667144984

Gene: NR1I2

Linked Data

• dbSNP Id: rs2055358320
• gnomAD v4: 3-119818356-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119818363dup , CM000665.2:g.119818363dup	GRCh38
NC_000003.11:g.119537210dup , CM000665.1:g.119537210dup	GRCh37
NC_000003.10:g.121019900dup	NCBI36
NG_011856.1:g.42880dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.*1151dup MANE Select	ENSP00000377319.3:n.*1151dup
ENST00000466380.6:c.*1151dup	ENSP00000420297.2:n.*1151dup
ENST00000337940.4:c.*1151dup	ENSP00000336528.4:n.*1151dup
ENST00000393716.6:c.*1151dup	ENSP00000377319.2:n.*1151dup
ENST00000466380.5:c.*1151dup	ENSP00000420297.1:n.*1151dup
ENST00000493757.1:n.2588dup
NM_003889.3:c.*1151dup	NP_003880.3:n.*1151dup
NM_022002.2:c.*1151dup	NP_071285.1:n.*1151dup
NM_033013.2:c.*1151dup	NP_148934.1:n.*1151dup
NM_003889.4:c.*1151dup MANE Select	NP_003880.3:n.*1151dup
NM_022002.3:c.*1151dup	NP_071285.1:n.*1151dup
NM_033013.3:c.*1151dup	NP_148934.1:n.*1151dup