Canonical Allele Identifier: CA412546935
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326474A>C (hg19) chrX:g.30308357A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308357A>C , CM000685.2:g.30308357A>C GRCh38
NC_000023.10:g.30326474A>C , CM000685.1:g.30326474A>C GRCh37
NC_000023.9:g.30236395A>C NCBI36
NG_009814.1:g.6022T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1007T>G MANE Select ENSP00000368253.4:p.Val336Gly
ENST00000378963.1:c.122T>G ENSP00000368246.1:p.Val41Gly
ENST00000378970.4:c.1007T>G ENSP00000368253.4:p.Val336Gly
NM_000475.4:c.1007T>G NP_000466.2:p.Val336Gly
NM_000475.5:c.1007T>G MANE Select NP_000466.2:p.Val336Gly
Search 100 bp 5'
Search 100 bp 3'