Canonical Allele Identifier: CA412546915
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308352T>A , CM000685.2:g.30308352T>A GRCh38
NC_000023.10:g.30326469T>A , CM000685.1:g.30326469T>A GRCh37
NC_000023.9:g.30236390T>A NCBI36
NG_009814.1:g.6027A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1012A>T MANE Select ENSP00000368253.4:p.Thr338Ser
ENST00000378963.1:c.127A>T ENSP00000368246.1:p.Thr43Ser
ENST00000378970.4:c.1012A>T ENSP00000368253.4:p.Thr338Ser
NM_000475.4:c.1012A>T NP_000466.2:p.Thr338Ser
NM_000475.5:c.1012A>T MANE Select NP_000466.2:p.Thr338Ser