Canonical Allele Identifier: CA1814482922
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947920C= , CM000670.2:g.118947920C= GRCh38
NC_000008.10:g.119960159C= , CM000670.1:g.119960159C= GRCh37
NC_000008.9:g.120029340C= NCBI36
NG_012202.1:g.9225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3872G= MANE Select ENSP00000297350.4:n.30+3872G=
ENST00000297350.8:c.30+3872G= ENSP00000297350.4:n.30+3872G=
ENST00000517352.1:c.30+3872G= ENSP00000427924.1:n.30+3872G=
NM_002546.3:c.30+3872G= NP_002537.3:n.30+3872G=
NM_002546.4:c.30+3872G= MANE Select NP_002537.3:n.30+3872G=
Search 100 bp 5'
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