Canonical Allele Identifier: CA2842742897
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308258dup , CM000685.2:g.30308258dup GRCh38
NC_000023.10:g.30326375dup , CM000685.1:g.30326375dup GRCh37
NC_000023.9:g.30236296dup NCBI36
NG_009814.1:g.6122dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1107dup MANE Select ENSP00000368253.4:p.Ser370GlufsTer19
ENST00000378963.1:c.222dup ENSP00000368246.1:p.Ser75GlufsTer19
ENST00000378970.4:c.1107dup ENSP00000368253.4:p.Ser370GlufsTer19
NM_000475.4:c.1107dup NP_000466.2:p.Ser370GlufsTer19
NM_000475.5:c.1107dup MANE Select NP_000466.2:p.Ser370GlufsTer19
Search 100 bp 5'
Search 100 bp 3'