Canonical Allele Identifier: CA354055559

Gene: NR1I2

Linked Data

• MyVariant Identifiers: chr3:g.119526136C>G (hg19) ; chr3:g.119807289C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807289C>G , CM000665.2:g.119807289C>G	GRCh38
NC_000003.11:g.119526136C>G , CM000665.1:g.119526136C>G	GRCh37
NC_000003.10:g.121008826C>G	NCBI36
NG_011856.1:g.31806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.39C>G MANE Select	ENSP00000377319.3:p.Asp13Glu
ENST00000466380.6:c.39C>G	ENSP00000420297.2:p.Asp13Glu
ENST00000648112.1:c.*62C>G	ENSP00000497876.1:n.*62C>G
ENST00000337940.4:c.156C>G	ENSP00000336528.4:p.Asp52Glu
ENST00000393716.6:c.39C>G	ENSP00000377319.2:p.Asp13Glu
ENST00000466380.5:c.39C>G	ENSP00000420297.1:p.Asp13Glu
ENST00000474090.1:n.327C>G
NM_003889.3:c.39C>G	NP_003880.3:p.Asp13Glu
NM_022002.2:c.156C>G	NP_071285.1:p.Asp52Glu
NM_033013.2:c.39C>G	NP_148934.1:p.Asp13Glu
NM_003889.4:c.39C>G MANE Select	NP_003880.3:p.Asp13Glu
NM_022002.3:c.156C>G	NP_071285.1:p.Asp52Glu
NM_033013.3:c.39C>G	NP_148934.1:p.Asp13Glu