Canonical Allele Identifier: CA184864853
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs550105482
gnomAD v3: 8-118939598-T-C
gnomAD v4: 8-118939598-T-C
MyVariant Identifiers: chr8:g.119951837T>C (hg19) chr8:g.118939598T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939598T>C , CM000670.2:g.118939598T>C GRCh38
NC_000008.10:g.119951837T>C , CM000670.1:g.119951837T>C GRCh37
NC_000008.9:g.120021018T>C NCBI36
NG_012202.1:g.17547A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.31-6298A>G MANE Select ENSP00000297350.4:n.31-6298A>G
ENST00000297350.8:c.31-6298A>G ENSP00000297350.4:n.31-6298A>G
ENST00000517352.1:c.31-6298A>G ENSP00000427924.1:n.31-6298A>G
NM_002546.3:c.31-6298A>G NP_002537.3:n.31-6298A>G
NM_002546.4:c.31-6298A>G MANE Select NP_002537.3:n.31-6298A>G
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