Canonical Allele Identifier: CA412548010
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308636A>T , CM000685.2:g.30308636A>T GRCh38
NC_000023.10:g.30326753A>T , CM000685.1:g.30326753A>T GRCh37
NC_000023.9:g.30236674A>T NCBI36
NG_009814.1:g.5743T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.728T>A MANE Select ENSP00000368253.4:p.Leu243Gln
ENST00000378970.4:c.728T>A ENSP00000368253.4:p.Leu243Gln
NM_000475.4:c.728T>A NP_000466.2:p.Leu243Gln
NM_000475.5:c.728T>A MANE Select NP_000466.2:p.Leu243Gln