Canonical Allele Identifier: CA354055635

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526156C>G (hg19) ; chr3:g.119807309C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807309C>G , CM000665.2:g.119807309C>G	GRCh38
NC_000003.11:g.119526156C>G , CM000665.1:g.119526156C>G	GRCh37
NC_000003.10:g.121008846C>G	NCBI36
NG_011856.1:g.31826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.59C>G MANE Select	ENSP00000377319.3:p.Thr20Arg
ENST00000466380.6:c.59C>G	ENSP00000420297.2:p.Thr20Arg
ENST00000648112.1:c.*82C>G	ENSP00000497876.1:n.*82C>G
ENST00000337940.4:c.176C>G	ENSP00000336528.4:p.Thr59Arg
ENST00000393716.6:c.59C>G	ENSP00000377319.2:p.Thr20Arg
ENST00000466380.5:c.59C>G	ENSP00000420297.1:p.Thr20Arg
ENST00000474090.1:n.347C>G
NM_003889.3:c.59C>G	NP_003880.3:p.Thr20Arg
NM_022002.2:c.176C>G	NP_071285.1:p.Thr59Arg
NM_033013.2:c.59C>G	NP_148934.1:p.Thr20Arg
NM_003889.4:c.59C>G MANE Select	NP_003880.3:p.Thr20Arg
NM_022002.3:c.176C>G	NP_071285.1:p.Thr59Arg
NM_033013.3:c.59C>G	NP_148934.1:p.Thr20Arg