Canonical Allele Identifier: CA1814482792
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947620C= , CM000670.2:g.118947620C= GRCh38
NC_000008.10:g.119959859C= , CM000670.1:g.119959859C= GRCh37
NC_000008.9:g.120029040C= NCBI36
NG_012202.1:g.9525G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.30+4172G= MANE Select ENSP00000297350.4:n.30+4172G=
ENST00000297350.8:c.30+4172G= ENSP00000297350.4:n.30+4172G=
ENST00000517352.1:c.30+4172G= ENSP00000427924.1:n.30+4172G=
NM_002546.3:c.30+4172G= NP_002537.3:n.30+4172G=
NM_002546.4:c.30+4172G= MANE Select NP_002537.3:n.30+4172G=
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