Canonical Allele Identifier: CA435219153

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526097C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807250C>T , CM000665.2:g.119807250C>T	GRCh38
NC_000003.11:g.119526097C>T , CM000665.1:g.119526097C>T	GRCh37
NC_000003.10:g.121008787C>T	NCBI36
NG_011856.1:g.31767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-1C>T MANE Select	ENSP00000377319.3:n.-1C>T
ENST00000466380.6:c.-1C>T	ENSP00000420297.2:n.-1C>T
ENST00000648112.1:c.*23C>T	ENSP00000497876.1:n.*23C>T
ENST00000337940.4:c.117C>T	ENSP00000336528.4:p.Asn39=
ENST00000393716.6:c.-1C>T	ENSP00000377319.2:n.-1C>T
ENST00000466380.5:c.-1C>T	ENSP00000420297.1:n.-1C>T
ENST00000474090.1:n.288C>T
NM_003889.3:c.-1C>T	NP_003880.3:n.-1C>T
NM_022002.2:c.117C>T	NP_071285.1:p.Asn39=
NM_033013.2:c.-1C>T	NP_148934.1:n.-1C>T
NM_003889.4:c.-1C>T MANE Select	NP_003880.3:n.-1C>T
NM_022002.3:c.117C>T	NP_071285.1:p.Asn39=
NM_033013.3:c.-1C>T	NP_148934.1:n.-1C>T