Canonical Allele Identifier: CA849995811
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1443906217
MyVariant Identifiers: chr8:g.23080029T>G (hg19) chr8:g.23222516T>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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