Canonical Allele Identifier: CA184864148
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs146084565
gnomAD v2: 8-119944967-A-C
gnomAD v3: 8-118932728-A-C
gnomAD v4: 8-118932728-A-C
MyVariant Identifiers: chr8:g.119944967A>C (hg19) chr8:g.118932728A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118932728A>C , CM000670.2:g.118932728A>C GRCh38
NC_000008.10:g.119944967A>C , CM000670.1:g.119944967A>C GRCh37
NC_000008.9:g.120014148A>C NCBI36
NG_012202.1:g.24417T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.400+203T>G MANE Select ENSP00000297350.4:n.400+203T>G
ENST00000297350.8:c.400+203T>G ENSP00000297350.4:n.400+203T>G
ENST00000517352.1:c.400+203T>G ENSP00000427924.1:n.400+203T>G
NM_002546.3:c.400+203T>G NP_002537.3:n.400+203T>G
NM_002546.4:c.400+203T>G MANE Select NP_002537.3:n.400+203T>G
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