Canonical Allele Identifier: CA2422040378

Gene: NR0B1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30308230G= , CM000685.2:g.30308230G=	GRCh38
NC_000023.10:g.30326347G= , CM000685.1:g.30326347G=	GRCh37
NC_000023.9:g.30236268G=	NCBI36
NG_009814.1:g.6149C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378970.5:c.1134C= MANE Select	ENSP00000368253.4:p.Tyr378=
ENST00000378963.1:c.249C=	ENSP00000368246.1:p.Tyr83=
ENST00000378970.4:c.1134C=	ENSP00000368253.4:p.Tyr378=
NM_000475.4:c.1134C=	NP_000466.2:p.Tyr378=
NM_000475.5:c.1134C= MANE Select	NP_000466.2:p.Tyr378=