Canonical Allele Identifier: CA371920575
Gene: TNFRSF11B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933029T>G , CM000670.2:g.118933029T>G GRCh38
NC_000008.10:g.119945268T>G , CM000670.1:g.119945268T>G GRCh37
NC_000008.9:g.120014449T>G NCBI36
NG_012202.1:g.24116A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.302A>C MANE Select ENSP00000297350.4:p.His101Pro
ENST00000297350.8:c.302A>C ENSP00000297350.4:p.His101Pro
ENST00000517352.1:c.302A>C ENSP00000427924.1:p.His101Pro
NM_002546.3:c.302A>C NP_002537.3:p.His101Pro
NM_002546.4:c.302A>C MANE Select NP_002537.3:p.His101Pro