Canonical Allele Identifier: CA354057549

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119530386T>C (hg19) ; chr3:g.119811539T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119811539T>C , CM000665.2:g.119811539T>C	GRCh38
NC_000003.11:g.119530386T>C , CM000665.1:g.119530386T>C	GRCh37
NC_000003.10:g.121013076T>C	NCBI36
NG_011856.1:g.36056T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.332T>C MANE Select	ENSP00000377319.3:p.Met111Thr
ENST00000466380.6:c.332T>C	ENSP00000420297.2:p.Met111Thr
ENST00000337940.4:c.449T>C	ENSP00000336528.4:p.Met150Thr
ENST00000393716.6:c.332T>C	ENSP00000377319.2:p.Met111Thr
ENST00000466380.5:c.332T>C	ENSP00000420297.1:p.Met111Thr
ENST00000493757.1:n.464T>C
NM_003889.3:c.332T>C	NP_003880.3:p.Met111Thr
NM_022002.2:c.449T>C	NP_071285.1:p.Met150Thr
NM_033013.2:c.332T>C	NP_148934.1:p.Met111Thr
NM_003889.4:c.332T>C MANE Select	NP_003880.3:p.Met111Thr
NM_022002.3:c.449T>C	NP_071285.1:p.Met150Thr
NM_033013.3:c.332T>C	NP_148934.1:p.Met111Thr