Canonical Allele Identifier: CA1814470713
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812346760
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118932736C>G , CM000670.2:g.118932736C>G GRCh38
NC_000008.10:g.119944975C>G , CM000670.1:g.119944975C>G GRCh37
NC_000008.9:g.120014156C>G NCBI36
NG_012202.1:g.24409G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.400+195G>C MANE Select ENSP00000297350.4:n.400+195G>C
ENST00000297350.8:c.400+195G>C ENSP00000297350.4:n.400+195G>C
ENST00000517352.1:c.400+195G>C ENSP00000427924.1:n.400+195G>C
NM_002546.3:c.400+195G>C NP_002537.3:n.400+195G>C
NM_002546.4:c.400+195G>C MANE Select NP_002537.3:n.400+195G>C
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