Canonical Allele Identifier: CA462984452
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs748687558
gnomAD v4: 8-118933052-G-C
MyVariant Identifiers: chr8:g.119945291G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933052G>C , CM000670.2:g.118933052G>C GRCh38
NC_000008.10:g.119945291G>C , CM000670.1:g.119945291G>C GRCh37
NC_000008.9:g.120014472G>C NCBI36
NG_012202.1:g.24093C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.279C>G MANE Select ENSP00000297350.4:p.Val93=
ENST00000297350.8:c.279C>G ENSP00000297350.4:p.Val93=
ENST00000517352.1:c.279C>G ENSP00000427924.1:p.Val93=
NM_002546.3:c.279C>G NP_002537.3:p.Val93=
NM_002546.4:c.279C>G MANE Select NP_002537.3:p.Val93=
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Search 100 bp 3'