Canonical Allele Identifier: CA354055813
Gene: NR1I2 HGNC NCBI

Linked Data

dbSNP Id: rs375785850

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807357G>C , CM000665.2:g.119807357G>C GRCh38
NC_000003.11:g.119526204G>C , CM000665.1:g.119526204G>C GRCh37
NC_000003.10:g.121008894G>C NCBI36
NG_011856.1:g.31874G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.107G>C MANE Select ENSP00000377319.3:p.Gly36Ala
ENST00000466380.6:c.107G>C ENSP00000420297.2:p.Gly36Ala
ENST00000648112.1:c.*130G>C ENSP00000497876.1:n.*130G>C
ENST00000337940.4:c.224G>C ENSP00000336528.4:p.Gly75Ala
ENST00000393716.6:c.107G>C ENSP00000377319.2:p.Gly36Ala
ENST00000466380.5:c.107G>C ENSP00000420297.1:p.Gly36Ala
ENST00000474090.1:n.395G>C
NM_003889.3:c.107G>C NP_003880.3:p.Gly36Ala
NM_022002.2:c.224G>C NP_071285.1:p.Gly75Ala
NM_033013.2:c.107G>C NP_148934.1:p.Gly36Ala
NM_003889.4:c.107G>C MANE Select NP_003880.3:p.Gly36Ala
NM_022002.3:c.224G>C NP_071285.1:p.Gly75Ala
NM_033013.3:c.107G>C NP_148934.1:p.Gly36Ala