Canonical Allele Identifier: CA846350223
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1192473405
gnomAD v3: 8-118947605-A-G
gnomAD v4: 8-118947605-A-G
MyVariant Identifiers: chr8:g.119959844A>G (hg19) chr8:g.118947605A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947605A>G , CM000670.2:g.118947605A>G GRCh38
NC_000008.10:g.119959844A>G , CM000670.1:g.119959844A>G GRCh37
NC_000008.9:g.120029025A>G NCBI36
NG_012202.1:g.9540T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.30+4187T>C MANE Select ENSP00000297350.4:n.30+4187T>C
ENST00000297350.8:c.30+4187T>C ENSP00000297350.4:n.30+4187T>C
ENST00000517352.1:c.30+4187T>C ENSP00000427924.1:n.30+4187T>C
NM_002546.3:c.30+4187T>C NP_002537.3:n.30+4187T>C
NM_002546.4:c.30+4187T>C MANE Select NP_002537.3:n.30+4187T>C
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