Canonical Allele Identifier: CA184865693
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs904922667
MyVariant Identifiers: chr8:g.119960104G>T (hg19) chr8:g.118947865G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947865G>T , CM000670.2:g.118947865G>T GRCh38
NC_000008.10:g.119960104G>T , CM000670.1:g.119960104G>T GRCh37
NC_000008.9:g.120029285G>T NCBI36
NG_012202.1:g.9280C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3927C>A MANE Select ENSP00000297350.4:n.30+3927C>A
ENST00000297350.8:c.30+3927C>A ENSP00000297350.4:n.30+3927C>A
ENST00000517352.1:c.30+3927C>A ENSP00000427924.1:n.30+3927C>A
NM_002546.3:c.30+3927C>A NP_002537.3:n.30+3927C>A
NM_002546.4:c.30+3927C>A MANE Select NP_002537.3:n.30+3927C>A
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