Canonical Allele Identifier: CA515946264
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326764G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308647G>A , CM000685.2:g.30308647G>A GRCh38
NC_000023.10:g.30326764G>A , CM000685.1:g.30326764G>A GRCh37
NC_000023.9:g.30236685G>A NCBI36
NG_009814.1:g.5732C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.717C>T MANE Select ENSP00000368253.4:p.Ser239=
ENST00000378970.4:c.717C>T ENSP00000368253.4:p.Ser239=
NM_000475.4:c.717C>T NP_000466.2:p.Ser239=
NM_000475.5:c.717C>T MANE Select NP_000466.2:p.Ser239=
Search 100 bp 5'
Search 100 bp 3'