Canonical Allele Identifier: CA354055522

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526126A>C (hg19) ; chr3:g.119807279A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807279A>C , CM000665.2:g.119807279A>C	GRCh38
NC_000003.11:g.119526126A>C , CM000665.1:g.119526126A>C	GRCh37
NC_000003.10:g.121008816A>C	NCBI36
NG_011856.1:g.31796A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.29A>C MANE Select	ENSP00000377319.3:p.Asn10Thr
ENST00000466380.6:c.29A>C	ENSP00000420297.2:p.Asn10Thr
ENST00000648112.1:c.*52A>C	ENSP00000497876.1:n.*52A>C
ENST00000337940.4:c.146A>C	ENSP00000336528.4:p.Asn49Thr
ENST00000393716.6:c.29A>C	ENSP00000377319.2:p.Asn10Thr
ENST00000466380.5:c.29A>C	ENSP00000420297.1:p.Asn10Thr
ENST00000474090.1:n.317A>C
NM_003889.3:c.29A>C	NP_003880.3:p.Asn10Thr
NM_022002.2:c.146A>C	NP_071285.1:p.Asn49Thr
NM_033013.2:c.29A>C	NP_148934.1:p.Asn10Thr
NM_003889.4:c.29A>C MANE Select	NP_003880.3:p.Asn10Thr
NM_022002.3:c.146A>C	NP_071285.1:p.Asn49Thr
NM_033013.3:c.29A>C	NP_148934.1:p.Asn10Thr