Canonical Allele Identifier: CA173948503
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1021603055
gnomAD v2: 8-23069647-C-T
gnomAD v4: 8-23212134-C-T
COSMIC: COSM3647351
MyVariant Identifiers: chr8:g.23069647C>T (hg19) chr8:g.23212134C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212134C>T , CM000670.2:g.23212134C>T GRCh38
NC_000008.10:g.23069647C>T , CM000670.1:g.23069647C>T GRCh37
NC_000008.9:g.23125592C>T NCBI36
NG_032107.1:g.18034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.385G>A MANE Select ENSP00000221132.3:p.Gly129Arg
ENST00000221132.7:c.385G>A ENSP00000221132.3:p.Gly129Arg
ENST00000524158.5:c.-222G>A ENSP00000428884.1:n.-222G>A
ENST00000613472.1:c.32-9475G>A ENSP00000480778.1:n.32-9475G>A
NM_003844.3:c.385G>A NP_003835.3:p.Gly129Arg
NM_003844.4:c.385G>A MANE Select NP_003835.3:p.Gly129Arg
Search 100 bp 5'
Search 100 bp 3'