Canonical Allele Identifier: CA412544263
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30304584-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304584T>A , CM000685.2:g.30304584T>A GRCh38
NC_000023.10:g.30322701T>A , CM000685.1:g.30322701T>A GRCh37
NC_000023.9:g.30232622T>A NCBI36
NG_009814.1:g.9795A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1408A>T MANE Select ENSP00000368253.4:p.Ile470Leu
ENST00000378970.4:c.1408A>T ENSP00000368253.4:p.Ile470Leu
NM_000475.4:c.1408A>T NP_000466.2:p.Ile470Leu
NM_000475.5:c.1408A>T MANE Select NP_000466.2:p.Ile470Leu