Canonical Allele Identifier: CA515946140
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326539G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308422G>C , CM000685.2:g.30308422G>C GRCh38
NC_000023.10:g.30326539G>C , CM000685.1:g.30326539G>C GRCh37
NC_000023.9:g.30236460G>C NCBI36
NG_009814.1:g.5957C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.942C>G MANE Select ENSP00000368253.4:p.Pro314=
ENST00000378963.1:c.57C>G ENSP00000368246.1:p.Pro19=
ENST00000378970.4:c.942C>G ENSP00000368253.4:p.Pro314=
NM_000475.4:c.942C>G NP_000466.2:p.Pro314=
NM_000475.5:c.942C>G MANE Select NP_000466.2:p.Pro314=
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