Canonical Allele Identifier: CA2422040292
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs1926554719

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308036C>G , CM000685.2:g.30308036C>G GRCh38
NC_000023.10:g.30326153C>G , CM000685.1:g.30326153C>G GRCh37
NC_000023.9:g.30236074C>G NCBI36
NG_009814.1:g.6343G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1168+160G>C MANE Select ENSP00000368253.4:n.1168+160G>C
ENST00000378963.1:c.283+160G>C ENSP00000368246.1:n.283+160G>C
ENST00000378970.4:c.1168+160G>C ENSP00000368253.4:n.1168+160G>C
NM_000475.4:c.1168+160G>C NP_000466.2:n.1168+160G>C
NM_000475.5:c.1168+160G>C MANE Select NP_000466.2:n.1168+160G>C