Canonical Allele Identifier: CA1396711479
Gene: NR1I2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119781188C= , CM000665.2:g.119781188C= GRCh38
NC_000003.11:g.119500035C= , CM000665.1:g.119500035C= GRCh37
NC_000003.10:g.120982725C= NCBI36
NG_011856.1:g.5705C=

Transcript Alleles

HGVS Amino-acid Change
NM_003889.3:c.-1135C= NP_003880.3:n.-1135C=
NM_033013.2:c.-1135C= NP_148934.1:n.-1135C=
ENST00000393716.6:c.-1135C= ENSP00000377319.2:n.-1135C=
ENST00000466380.5:c.-1135C= ENSP00000420297.1:n.-1135C=
ENST00000466380.6:c.-1135C= ENSP00000420297.2:n.-1135C=
ENST00000648112.1:c.*2-26041C= ENSP00000497876.1:n.*2-26041C=