Canonical Allele Identifier: CA849995815
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1443906217
gnomAD v3: 8-23222516-T-C
gnomAD v4: 8-23222516-T-C
MyVariant Identifiers: chr8:g.23080029T>C (hg19) chr8:g.23222516T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222516T>C , CM000670.2:g.23222516T>C GRCh38
NC_000008.10:g.23080029T>C , CM000670.1:g.23080029T>C GRCh37
NC_000008.9:g.23135974T>C NCBI36
NG_032107.1:g.7652A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2240A>G MANE Select ENSP00000221132.3:n.306+2240A>G
ENST00000221132.7:c.306+2240A>G ENSP00000221132.3:n.306+2240A>G
ENST00000524158.5:c.-301+1917A>G ENSP00000428884.1:n.-301+1917A>G
ENST00000613472.1:c.31+2515A>G ENSP00000480778.1:n.31+2515A>G
NM_003844.3:c.306+2240A>G NP_003835.3:n.306+2240A>G
NM_003844.4:c.306+2240A>G MANE Select NP_003835.3:n.306+2240A>G
Search 100 bp 5'
Search 100 bp 3'