Canonical Allele Identifier: CA2693382728
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30304556-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304556G>A , CM000685.2:g.30304556G>A GRCh38
NC_000023.10:g.30322673G>A , CM000685.1:g.30322673G>A GRCh37
NC_000023.9:g.30232594G>A NCBI36
NG_009814.1:g.9823C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*23C>T MANE Select ENSP00000368253.4:n.*23C>T
ENST00000378970.4:c.*23C>T ENSP00000368253.4:n.*23C>T
NM_000475.4:c.*23C>T NP_000466.2:n.*23C>T
NM_000475.5:c.*23C>T MANE Select NP_000466.2:n.*23C>T