Canonical Allele Identifier: CA354055818

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526206G>T (hg19) ; chr3:g.119807359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807359G>T , CM000665.2:g.119807359G>T	GRCh38
NC_000003.11:g.119526206G>T , CM000665.1:g.119526206G>T	GRCh37
NC_000003.10:g.121008896G>T	NCBI36
NG_011856.1:g.31876G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.109G>T MANE Select	ENSP00000377319.3:p.Gly37Cys
ENST00000466380.6:c.109G>T	ENSP00000420297.2:p.Gly37Cys
ENST00000648112.1:c.*132G>T	ENSP00000497876.1:n.*132G>T
ENST00000337940.4:c.226G>T	ENSP00000336528.4:p.Gly76Cys
ENST00000393716.6:c.109G>T	ENSP00000377319.2:p.Gly37Cys
ENST00000466380.5:c.109G>T	ENSP00000420297.1:p.Gly37Cys
ENST00000474090.1:n.397G>T
NM_003889.3:c.109G>T	NP_003880.3:p.Gly37Cys
NM_022002.2:c.226G>T	NP_071285.1:p.Gly76Cys
NM_033013.2:c.109G>T	NP_148934.1:p.Gly37Cys
NM_003889.4:c.109G>T MANE Select	NP_003880.3:p.Gly37Cys
NM_022002.3:c.226G>T	NP_071285.1:p.Gly76Cys
NM_033013.3:c.109G>T	NP_148934.1:p.Gly37Cys