Canonical Allele Identifier: CA462984375
Gene: TNFRSF11B HGNC NCBI

Linked Data

gnomAD v4: 8-118933031-G-A
MyVariant Identifiers: chr8:g.119945270G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933031G>A , CM000670.2:g.118933031G>A GRCh38
NC_000008.10:g.119945270G>A , CM000670.1:g.119945270G>A GRCh37
NC_000008.9:g.120014451G>A NCBI36
NG_012202.1:g.24114C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.300C>T MANE Select ENSP00000297350.4:p.Thr100=
ENST00000297350.8:c.300C>T ENSP00000297350.4:p.Thr100=
ENST00000517352.1:c.300C>T ENSP00000427924.1:p.Thr100=
NM_002546.3:c.300C>T NP_002537.3:p.Thr100=
NM_002546.4:c.300C>T MANE Select NP_002537.3:p.Thr100=
Search 100 bp 5'
Search 100 bp 3'