Canonical Allele Identifier: CA1814482933
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812590911
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947950_118947953del , CM000670.2:g.118947950_118947953del GRCh38
NC_000008.10:g.119960189_119960192del , CM000670.1:g.119960189_119960192del GRCh37
NC_000008.9:g.120029370_120029373del NCBI36
NG_012202.1:g.9194_9197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3841_30+3844del MANE Select ENSP00000297350.4:n.30+3841_30+3844del
ENST00000297350.8:c.30+3841_30+3844del ENSP00000297350.4:n.30+3841_30+3844del
ENST00000517352.1:c.30+3841_30+3844del ENSP00000427924.1:n.30+3841_30+3844del
NM_002546.3:c.30+3841_30+3844del NP_002537.3:n.30+3841_30+3844del
NM_002546.4:c.30+3841_30+3844del MANE Select NP_002537.3:n.30+3841_30+3844del
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