Canonical Allele Identifier: CA12819766
Gene: TNFRSF11B HGNC NCBI
dbSNP:
1032128
gnomAD v2:
8:119951773 G / A
gnomAD v3:
8:118939534 G / A
gnomAD v4:
chr8-118939534-G-A
Joint Max Group AF 0.59226637 (EAS)
Genomes Max Group AF 0.59226637 (EAS)
MyVariant.info:
GRCh38 chr8:g.118939534G>A
GRCh37 chr8:g.119951773G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939534G>A , CM000670.2:g.118939534G>A GRCh38
NC_000008.10:g.119951773G>A , CM000670.1:g.119951773G>A GRCh37
NC_000008.9:g.120020954G>A NCBI36
NG_012202.1:g.17611C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.31-6234C>T MANE Select ENSP00000297350.4:n.31-6234C>T
ENST00000297350.8:c.31-6234C>T ENSP00000297350.4:n.31-6234C>T
ENST00000517352.1:c.31-6234C>T ENSP00000427924.1:n.31-6234C>T
NM_002546.3:c.31-6234C>T NP_002537.3:n.31-6234C>T
NM_002546.4:c.31-6234C>T MANE Select NP_002537.3:n.31-6234C>T
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