Canonical Allele Identifier: CA11374764

Gene: NR1I2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119784198C>T , CM000665.2:g.119784198C>T	GRCh38
NC_000003.11:g.119503045C>T , CM000665.1:g.119503045C>T	GRCh37
NC_000003.10:g.120985735C>T	NCBI36
NG_011856.1:g.8715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-23+1898C>T MANE Select	ENSP00000377319.3:n.-23+1898C>T
ENST00000466380.6:c.-23+1898C>T	ENSP00000420297.2:n.-23+1898C>T
ENST00000648112.1:c.*2-23031C>T	ENSP00000497876.1:n.*2-23031C>T
ENST00000337940.4:c.95+1346C>T	ENSP00000336528.4:n.95+1346C>T
ENST00000393716.6:c.-23+1898C>T	ENSP00000377319.2:n.-23+1898C>T
ENST00000466380.5:c.-23+1898C>T	ENSP00000420297.1:n.-23+1898C>T
ENST00000474090.1:n.266+1898C>T
NM_003889.3:c.-23+1898C>T	NP_003880.3:n.-23+1898C>T
NM_022002.2:c.95+1346C>T	NP_071285.1:n.95+1346C>T
NM_033013.2:c.-23+1898C>T	NP_148934.1:n.-23+1898C>T
NM_003889.4:c.-23+1898C>T MANE Select	NP_003880.3:n.-23+1898C>T
NM_022002.3:c.95+1346C>T	NP_071285.1:n.95+1346C>T
NM_033013.3:c.-23+1898C>T	NP_148934.1:n.-23+1898C>T