Canonical Allele Identifier: CA412545316
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30322865G>A (hg19) chrX:g.30304748G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304748G>A , CM000685.2:g.30304748G>A GRCh38
NC_000023.10:g.30322865G>A , CM000685.1:g.30322865G>A GRCh37
NC_000023.9:g.30232786G>A NCBI36
NG_009814.1:g.9631C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1244C>T MANE Select ENSP00000368253.4:p.Thr415Ile
ENST00000378970.4:c.1244C>T ENSP00000368253.4:p.Thr415Ile
NM_000475.4:c.1244C>T NP_000466.2:p.Thr415Ile
NM_000475.5:c.1244C>T MANE Select NP_000466.2:p.Thr415Ile
Search 100 bp 5'
Search 100 bp 3'