Canonical Allele Identifier: CA2422039206
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304723A= , CM000685.2:g.30304723A= GRCh38
NC_000023.10:g.30322840A= , CM000685.1:g.30322840A= GRCh37
NC_000023.9:g.30232761A= NCBI36
NG_009814.1:g.9656T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1269T= MANE Select ENSP00000368253.4:p.His423=
ENST00000378970.4:c.1269T= ENSP00000368253.4:p.His423=
NM_000475.4:c.1269T= NP_000466.2:p.His423=
NM_000475.5:c.1269T= MANE Select NP_000466.2:p.His423=