Canonical Allele Identifier: CA371920671
Gene: TNFRSF11B HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119945309G>C (hg19) chr8:g.118933070G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933070G>C , CM000670.2:g.118933070G>C GRCh38
NC_000008.10:g.119945309G>C , CM000670.1:g.119945309G>C GRCh37
NC_000008.9:g.120014490G>C NCBI36
NG_012202.1:g.24075C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.261C>G MANE Select ENSP00000297350.4:p.Cys87Trp
ENST00000297350.8:c.261C>G ENSP00000297350.4:p.Cys87Trp
ENST00000517352.1:c.261C>G ENSP00000427924.1:p.Cys87Trp
NM_002546.3:c.261C>G NP_002537.3:p.Cys87Trp
NM_002546.4:c.261C>G MANE Select NP_002537.3:p.Cys87Trp
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