Canonical Allele Identifier: CA2422040500
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308621A= , CM000685.2:g.30308621A= GRCh38
NC_000023.10:g.30326738A= , CM000685.1:g.30326738A= GRCh37
NC_000023.9:g.30236659A= NCBI36
NG_009814.1:g.5758T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.743T= MANE Select ENSP00000368253.4:p.Leu248=
ENST00000378970.4:c.743T= ENSP00000368253.4:p.Leu248=
NM_000475.4:c.743T= NP_000466.2:p.Leu248=
NM_000475.5:c.743T= MANE Select NP_000466.2:p.Leu248=