Canonical Allele Identifier: CA1118413409
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812583940
gnomAD v3: 8-118947594-G-C
gnomAD v4: 8-118947594-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947594G>C , CM000670.2:g.118947594G>C GRCh38
NC_000008.10:g.119959833G>C , CM000670.1:g.119959833G>C GRCh37
NC_000008.9:g.120029014G>C NCBI36
NG_012202.1:g.9551C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.30+4198C>G MANE Select ENSP00000297350.4:n.30+4198C>G
ENST00000297350.8:c.30+4198C>G ENSP00000297350.4:n.30+4198C>G
ENST00000517352.1:c.30+4198C>G ENSP00000427924.1:n.30+4198C>G
NM_002546.3:c.30+4198C>G NP_002537.3:n.30+4198C>G
NM_002546.4:c.30+4198C>G MANE Select NP_002537.3:n.30+4198C>G
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