Canonical Allele Identifier: CA371920652
Gene: TNFRSF11B HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119945301A>T (hg19) chr8:g.118933062A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933062A>T , CM000670.2:g.118933062A>T GRCh38
NC_000008.10:g.119945301A>T , CM000670.1:g.119945301A>T GRCh37
NC_000008.9:g.120014482A>T NCBI36
NG_012202.1:g.24083T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.269T>A MANE Select ENSP00000297350.4:p.Leu90Gln
ENST00000297350.8:c.269T>A ENSP00000297350.4:p.Leu90Gln
ENST00000517352.1:c.269T>A ENSP00000427924.1:p.Leu90Gln
NM_002546.3:c.269T>A NP_002537.3:p.Leu90Gln
NM_002546.4:c.269T>A MANE Select NP_002537.3:p.Leu90Gln
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Search 100 bp 3'