Canonical Allele Identifier: CA2695232135

Gene: NR0B1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30304611dup , CM000685.2:g.30304611dup	GRCh38
NC_000023.10:g.30322728dup , CM000685.1:g.30322728dup	GRCh37
NC_000023.9:g.30232649dup	NCBI36
NG_009814.1:g.9768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378970.5:c.1381dup MANE Select	ENSP00000368253.4:p.Met461AsnfsTer?
ENST00000378970.4:c.1381dup	ENSP00000368253.4:p.Met461AsnfsTer?
NM_000475.4:c.1381dup	NP_000466.2:p.Met461AsnfsTer?
NM_000475.5:c.1381dup MANE Select	NP_000466.2:p.Met461AsnfsTer?