Canonical Allele Identifier: CA184865692
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs530264704
gnomAD v3: 8-118947841-G-A
gnomAD v4: 8-118947841-G-A
MyVariant Identifiers: chr8:g.119960080G>A (hg19) chr8:g.118947841G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947841G>A , CM000670.2:g.118947841G>A GRCh38
NC_000008.10:g.119960080G>A , CM000670.1:g.119960080G>A GRCh37
NC_000008.9:g.120029261G>A NCBI36
NG_012202.1:g.9304C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3951C>T MANE Select ENSP00000297350.4:n.30+3951C>T
ENST00000297350.8:c.30+3951C>T ENSP00000297350.4:n.30+3951C>T
ENST00000517352.1:c.30+3951C>T ENSP00000427924.1:n.30+3951C>T
NM_002546.3:c.30+3951C>T NP_002537.3:n.30+3951C>T
NM_002546.4:c.30+3951C>T MANE Select NP_002537.3:n.30+3951C>T
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