Canonical Allele Identifier: CA371920888

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945403G>C (hg19) ; chr8:g.118933164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118933164G>C , CM000670.2:g.118933164G>C	GRCh38
NC_000008.10:g.119945403G>C , CM000670.1:g.119945403G>C	GRCh37
NC_000008.9:g.120014584G>C	NCBI36
NG_012202.1:g.23981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.167C>G MANE Select	ENSP00000297350.4:p.Ala56Gly
ENST00000297350.8:c.167C>G	ENSP00000297350.4:p.Ala56Gly
ENST00000517352.1:c.167C>G	ENSP00000427924.1:p.Ala56Gly
NM_002546.3:c.167C>G	NP_002537.3:p.Ala56Gly
NM_002546.4:c.167C>G MANE Select	NP_002537.3:p.Ala56Gly