Canonical Allele Identifier: CA1814470729
Gene: TNFRSF11B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118932759G= , CM000670.2:g.118932759G= GRCh38
NC_000008.10:g.119944998G= , CM000670.1:g.119944998G= GRCh37
NC_000008.9:g.120014179G= NCBI36
NG_012202.1:g.24386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.400+172C= MANE Select ENSP00000297350.4:n.400+172C=
ENST00000297350.8:c.400+172C= ENSP00000297350.4:n.400+172C=
ENST00000517352.1:c.400+172C= ENSP00000427924.1:n.400+172C=
NM_002546.3:c.400+172C= NP_002537.3:n.400+172C=
NM_002546.4:c.400+172C= MANE Select NP_002537.3:n.400+172C=