Canonical Allele Identifier: CA2422039139
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304511T= , CM000685.2:g.30304511T= GRCh38
NC_000023.10:g.30322628T= , CM000685.1:g.30322628T= GRCh37
NC_000023.9:g.30232549T= NCBI36
NG_009814.1:g.9868A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*68A= MANE Select ENSP00000368253.4:n.*68A=
ENST00000378970.4:c.*68A= ENSP00000368253.4:n.*68A=
NM_000475.4:c.*68A= NP_000466.2:n.*68A=
NM_000475.5:c.*68A= MANE Select NP_000466.2:n.*68A=
Search 100 bp 5'
Search 100 bp 3'