Canonical Allele Identifier: CA412544418
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30322765G>T (hg19) chrX:g.30304648G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304648G>T , CM000685.2:g.30304648G>T GRCh38
NC_000023.10:g.30322765G>T , CM000685.1:g.30322765G>T GRCh37
NC_000023.9:g.30232686G>T NCBI36
NG_009814.1:g.9731C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1344C>A MANE Select ENSP00000368253.4:p.Phe448Leu
ENST00000378970.4:c.1344C>A ENSP00000368253.4:p.Phe448Leu
NM_000475.4:c.1344C>A NP_000466.2:p.Phe448Leu
NM_000475.5:c.1344C>A MANE Select NP_000466.2:p.Phe448Leu
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