Canonical Allele Identifier: CA370569029
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1214440201
MyVariant Identifiers: chr8:g.23049371A>G (hg19) chr8:g.23191858A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191858A>G , CM000670.2:g.23191858A>G GRCh38
NC_000008.10:g.23049371A>G , CM000670.1:g.23049371A>G GRCh37
NC_000008.9:g.23105316A>G NCBI36
NG_032107.1:g.38310T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1243T>C MANE Select ENSP00000221132.3:p.Trp415Arg
ENST00000221132.7:c.1243T>C ENSP00000221132.3:p.Trp415Arg
ENST00000519862.1:n.298T>C
ENST00000613472.1:c.769T>C ENSP00000480778.1:p.Trp257Arg
NM_003844.3:c.1243T>C NP_003835.3:p.Trp415Arg
NM_003844.4:c.1243T>C MANE Select NP_003835.3:p.Trp415Arg
Search 100 bp 5'
Search 100 bp 3'