Canonical Allele Identifier: CA1814471116
Gene: TNFRSF11B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933047T= , CM000670.2:g.118933047T= GRCh38
NC_000008.10:g.119945286T= , CM000670.1:g.119945286T= GRCh37
NC_000008.9:g.120014467T= NCBI36
NG_012202.1:g.24098A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.284A= MANE Select ENSP00000297350.4:p.Gln95=
ENST00000297350.8:c.284A= ENSP00000297350.4:p.Gln95=
ENST00000517352.1:c.284A= ENSP00000427924.1:p.Gln95=
NM_002546.3:c.284A= NP_002537.3:p.Gln95=
NM_002546.4:c.284A= MANE Select NP_002537.3:p.Gln95=