Canonical Allele Identifier: CA846345975
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1365493454
gnomAD v3: 8-118939462-A-G
gnomAD v4: 8-118939462-A-G
MyVariant Identifiers: chr8:g.119951701A>G (hg19) chr8:g.118939462A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939462A>G , CM000670.2:g.118939462A>G GRCh38
NC_000008.10:g.119951701A>G , CM000670.1:g.119951701A>G GRCh37
NC_000008.9:g.120020882A>G NCBI36
NG_012202.1:g.17683T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6162T>C MANE Select ENSP00000297350.4:n.31-6162T>C
ENST00000297350.8:c.31-6162T>C ENSP00000297350.4:n.31-6162T>C
ENST00000517352.1:c.31-6162T>C ENSP00000427924.1:n.31-6162T>C
NM_002546.3:c.31-6162T>C NP_002537.3:n.31-6162T>C
NM_002546.4:c.31-6162T>C MANE Select NP_002537.3:n.31-6162T>C
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