Canonical Allele Identifier: CA248435

Gene: TNFRSF10A-DT

Linked Data

• ClinVar Variation Id: 162169
• ClinVar RCV Id: RCV000190305
• dbSNP Id: rs13278062
• gnomAD v2: 8-23082971-G-T
• gnomAD v3: 8-23225458-G-T
• gnomAD v4: 8-23225458-G-T
• MyVariant Identifiers: chr8:g.23082971G>T (hg19) ; chr8:g.23225458G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23225458G>T , CM000670.2:g.23225458G>T	GRCh38
NC_000008.10:g.23082971G>T , CM000670.1:g.23082971G>T	GRCh37
NC_000008.9:g.23138916G>T	NCBI36
NG_032107.1:g.4710C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_033928.1:n.238G>T