Canonical Allele Identifier: CA584550560
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1487879802
gnomAD v2: 8-119951753-G-A
gnomAD v3: 8-118939514-G-A
gnomAD v4: 8-118939514-G-A
MyVariant Identifiers: chr8:g.119951753G>A (hg19) chr8:g.118939514G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939514G>A , CM000670.2:g.118939514G>A GRCh38
NC_000008.10:g.119951753G>A , CM000670.1:g.119951753G>A GRCh37
NC_000008.9:g.120020934G>A NCBI36
NG_012202.1:g.17631C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.31-6214C>T MANE Select ENSP00000297350.4:n.31-6214C>T
ENST00000297350.8:c.31-6214C>T ENSP00000297350.4:n.31-6214C>T
ENST00000517352.1:c.31-6214C>T ENSP00000427924.1:n.31-6214C>T
NM_002546.3:c.31-6214C>T NP_002537.3:n.31-6214C>T
NM_002546.4:c.31-6214C>T MANE Select NP_002537.3:n.31-6214C>T
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