Canonical Allele Identifier: CA2693383089
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30308055-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308055T>C , CM000685.2:g.30308055T>C GRCh38
NC_000023.10:g.30326172T>C , CM000685.1:g.30326172T>C GRCh37
NC_000023.9:g.30236093T>C NCBI36
NG_009814.1:g.6324A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1168+141A>G MANE Select ENSP00000368253.4:n.1168+141A>G
ENST00000378963.1:c.283+141A>G ENSP00000368246.1:n.283+141A>G
ENST00000378970.4:c.1168+141A>G ENSP00000368253.4:n.1168+141A>G
NM_000475.4:c.1168+141A>G NP_000466.2:n.1168+141A>G
NM_000475.5:c.1168+141A>G MANE Select NP_000466.2:n.1168+141A>G