Canonical Allele Identifier: CA846350419
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1312819455
MyVariant Identifiers: chr8:g.119960150_119960157del (hg19) chr8:g.118947911_118947918del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947915_118947922del , CM000670.2:g.118947915_118947922del GRCh38
NC_000008.10:g.119960154_119960161del , CM000670.1:g.119960154_119960161del GRCh37
NC_000008.9:g.120029335_120029342del NCBI36
NG_012202.1:g.9227_9234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3874_30+3881del MANE Select ENSP00000297350.4:n.30+3874_30+3881del
ENST00000297350.8:c.30+3874_30+3881del ENSP00000297350.4:n.30+3874_30+3881del
ENST00000517352.1:c.30+3874_30+3881del ENSP00000427924.1:n.30+3874_30+3881del
NM_002546.3:c.30+3874_30+3881del NP_002537.3:n.30+3874_30+3881del
NM_002546.4:c.30+3874_30+3881del MANE Select NP_002537.3:n.30+3874_30+3881del
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