Canonical Allele Identifier: CA412544299
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30322715A>C (hg19) chrX:g.30304598A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304598A>C , CM000685.2:g.30304598A>C GRCh38
NC_000023.10:g.30322715A>C , CM000685.1:g.30322715A>C GRCh37
NC_000023.9:g.30232636A>C NCBI36
NG_009814.1:g.9781T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1394T>G MANE Select ENSP00000368253.4:p.Met465Arg
ENST00000378970.4:c.1394T>G ENSP00000368253.4:p.Met465Arg
NM_000475.4:c.1394T>G NP_000466.2:p.Met465Arg
NM_000475.5:c.1394T>G MANE Select NP_000466.2:p.Met465Arg
Search 100 bp 5'
Search 100 bp 3'