Canonical Allele Identifier: CA435219093

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526085C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807238C>G , CM000665.2:g.119807238C>G	GRCh38
NC_000003.11:g.119526085C>G , CM000665.1:g.119526085C>G	GRCh37
NC_000003.10:g.121008775C>G	NCBI36
NG_011856.1:g.31755C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-13C>G MANE Select	ENSP00000377319.3:n.-13C>G
ENST00000466380.6:c.-13C>G	ENSP00000420297.2:n.-13C>G
ENST00000648112.1:c.*11C>G	ENSP00000497876.1:n.*11C>G
ENST00000337940.4:c.105C>G	ENSP00000336528.4:p.Gly35=
ENST00000393716.6:c.-13C>G	ENSP00000377319.2:n.-13C>G
ENST00000466380.5:c.-13C>G	ENSP00000420297.1:n.-13C>G
ENST00000474090.1:n.276C>G
NM_003889.3:c.-13C>G	NP_003880.3:n.-13C>G
NM_022002.2:c.105C>G	NP_071285.1:p.Gly35=
NM_033013.2:c.-13C>G	NP_148934.1:n.-13C>G
NM_003889.4:c.-13C>G MANE Select	NP_003880.3:n.-13C>G
NM_022002.3:c.105C>G	NP_071285.1:p.Gly35=
NM_033013.3:c.-13C>G	NP_148934.1:n.-13C>G