Canonical Allele Identifier: CA2539729381
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939516_118939521del , CM000670.2:g.118939516_118939521del GRCh38
NC_000008.10:g.119951755_119951760del , CM000670.1:g.119951755_119951760del GRCh37
NC_000008.9:g.120020936_120020941del NCBI36
NG_012202.1:g.17624_17629del

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6221_31-6216del MANE Select ENSP00000297350.4:n.31-6221_31-6216del
ENST00000297350.8:c.31-6221_31-6216del ENSP00000297350.4:n.31-6221_31-6216del
ENST00000517352.1:c.31-6221_31-6216del ENSP00000427924.1:n.31-6221_31-6216del
NM_002546.3:c.31-6221_31-6216del NP_002537.3:n.31-6221_31-6216del
NM_002546.4:c.31-6221_31-6216del MANE Select NP_002537.3:n.31-6221_31-6216del
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