Canonical Allele Identifier: CA412544387

Gene: NR0B1

Linked Data

• MyVariant Identifiers: chrX:g.30322751A>G (hg19) ; chrX:g.30304634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30304634A>G , CM000685.2:g.30304634A>G	GRCh38
NC_000023.10:g.30322751A>G , CM000685.1:g.30322751A>G	GRCh37
NC_000023.9:g.30232672A>G	NCBI36
NG_009814.1:g.9745T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378970.5:c.1358T>C MANE Select	ENSP00000368253.4:p.Ile453Thr
ENST00000378970.4:c.1358T>C	ENSP00000368253.4:p.Ile453Thr
NM_000475.4:c.1358T>C	NP_000466.2:p.Ile453Thr
NM_000475.5:c.1358T>C MANE Select	NP_000466.2:p.Ile453Thr