Canonical Allele Identifier: CA370576651
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1800898445
gnomAD v4: 8-23200718-C-T
MyVariant Identifiers: chr8:g.23058231C>T (hg19) chr8:g.23200718C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23200718C>T , CM000670.2:g.23200718C>T GRCh38
NC_000008.10:g.23058231C>T , CM000670.1:g.23058231C>T GRCh37
NC_000008.9:g.23114176C>T NCBI36
NG_032107.1:g.29450G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.672G>A MANE Select ENSP00000221132.3:p.Trp224Ter
ENST00000221132.7:c.672G>A ENSP00000221132.3:p.Trp224Ter
ENST00000524158.5:c.66G>A ENSP00000428884.1:p.Trp22Ter
ENST00000613472.1:c.198G>A ENSP00000480778.1:p.Trp66Ter
NM_003844.3:c.672G>A NP_003835.3:p.Trp224Ter
NM_003844.4:c.672G>A MANE Select NP_003835.3:p.Trp224Ter
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