Canonical Allele Identifier: CA412545228
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30322845G>T (hg19) chrX:g.30304728G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304728G>T , CM000685.2:g.30304728G>T GRCh38
NC_000023.10:g.30322845G>T , CM000685.1:g.30322845G>T GRCh37
NC_000023.9:g.30232766G>T NCBI36
NG_009814.1:g.9651C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1264C>A MANE Select ENSP00000368253.4:p.Pro422Thr
ENST00000378970.4:c.1264C>A ENSP00000368253.4:p.Pro422Thr
NM_000475.4:c.1264C>A NP_000466.2:p.Pro422Thr
NM_000475.5:c.1264C>A MANE Select NP_000466.2:p.Pro422Thr
Search 100 bp 5'
Search 100 bp 3'