Canonical Allele Identifier: CA412546773
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308321T>C , CM000685.2:g.30308321T>C GRCh38
NC_000023.10:g.30326438T>C , CM000685.1:g.30326438T>C GRCh37
NC_000023.9:g.30236359T>C NCBI36
NG_009814.1:g.6058A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1043A>G MANE Select ENSP00000368253.4:p.Glu348Gly
ENST00000378963.1:c.158A>G ENSP00000368246.1:p.Glu53Gly
ENST00000378970.4:c.1043A>G ENSP00000368253.4:p.Glu348Gly
NM_000475.4:c.1043A>G NP_000466.2:p.Glu348Gly
NM_000475.5:c.1043A>G MANE Select NP_000466.2:p.Glu348Gly