Canonical Allele Identifier: CA371920564
Gene: TNFRSF11B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933025G>C , CM000670.2:g.118933025G>C GRCh38
NC_000008.10:g.119945264G>C , CM000670.1:g.119945264G>C GRCh37
NC_000008.9:g.120014445G>C NCBI36
NG_012202.1:g.24120C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.306C>G MANE Select ENSP00000297350.4:p.Asn102Lys
ENST00000297350.8:c.306C>G ENSP00000297350.4:p.Asn102Lys
ENST00000517352.1:c.306C>G ENSP00000427924.1:p.Asn102Lys
NM_002546.3:c.306C>G NP_002537.3:p.Asn102Lys
NM_002546.4:c.306C>G MANE Select NP_002537.3:p.Asn102Lys