Canonical Allele Identifier: CA2422039147
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs1926484648
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304538A>G , CM000685.2:g.30304538A>G GRCh38
NC_000023.10:g.30322655A>G , CM000685.1:g.30322655A>G GRCh37
NC_000023.9:g.30232576A>G NCBI36
NG_009814.1:g.9841T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*41T>C MANE Select ENSP00000368253.4:n.*41T>C
ENST00000378970.4:c.*41T>C ENSP00000368253.4:n.*41T>C
NM_000475.4:c.*41T>C NP_000466.2:n.*41T>C
NM_000475.5:c.*41T>C MANE Select NP_000466.2:n.*41T>C
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