Canonical Allele Identifier: CA11452819

Gene: NR1I2

Linked Data

• dbSNP Id: rs6785049
• gnomAD v2: 3-119533733-G-A
• gnomAD v3: 3-119814886-G-A
• gnomAD v4: 3-119814886-G-A
• MyVariant Identifiers: chr3:g.119533733G>A (hg19) ; chr3:g.119814886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119814886G>A , CM000665.2:g.119814886G>A	GRCh38
NC_000003.11:g.119533733G>A , CM000665.1:g.119533733G>A	GRCh37
NC_000003.10:g.121016423G>A	NCBI36
NG_011856.1:g.39403G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000393716.8:c.795-93G>A MANE Select	ENSP00000377319.3:n.795-93G>A
ENST00000466380.6:c.684-93G>A	ENSP00000420297.2:n.684-93G>A
ENST00000337940.4:c.912-93G>A	ENSP00000336528.4:n.912-93G>A
ENST00000393716.6:c.795-93G>A	ENSP00000377319.2:n.795-93G>A
ENST00000466380.5:c.684-93G>A	ENSP00000420297.1:n.684-93G>A
ENST00000493757.1:n.927-93G>A
NM_003889.3:c.795-93G>A	NP_003880.3:n.795-93G>A
NM_022002.2:c.912-93G>A	NP_071285.1:n.912-93G>A
NM_033013.2:c.684-93G>A	NP_148934.1:n.684-93G>A
NM_003889.4:c.795-93G>A MANE Select	NP_003880.3:n.795-93G>A
NM_022002.3:c.912-93G>A	NP_071285.1:n.912-93G>A
NM_033013.3:c.684-93G>A	NP_148934.1:n.684-93G>A