Canonical Allele Identifier: CA2422040420
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308368C= , CM000685.2:g.30308368C= GRCh38
NC_000023.10:g.30326485C= , CM000685.1:g.30326485C= GRCh37
NC_000023.9:g.30236406C= NCBI36
NG_009814.1:g.6011G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.996G= MANE Select ENSP00000368253.4:p.Glu332=
ENST00000378963.1:c.111G= ENSP00000368246.1:p.Glu37=
ENST00000378970.4:c.996G= ENSP00000368253.4:p.Glu332=
NM_000475.4:c.996G= NP_000466.2:p.Glu332=
NM_000475.5:c.996G= MANE Select NP_000466.2:p.Glu332=
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