Canonical Allele Identifier: CA4674936
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs776892107
ExAC: 8:23069604 A / T
gnomAD v2: 8-23069604-A-T
gnomAD v4: 8-23212091-A-T
MyVariant Identifiers: chr8:g.23069604A>T (hg19) chr8:g.23212091A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212091A>T , CM000670.2:g.23212091A>T GRCh38
NC_000008.10:g.23069604A>T , CM000670.1:g.23069604A>T GRCh37
NC_000008.9:g.23125549A>T NCBI36
NG_032107.1:g.18077T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+25T>A MANE Select ENSP00000221132.3:n.403+25T>A
ENST00000221132.7:c.403+25T>A ENSP00000221132.3:n.403+25T>A
ENST00000524158.5:c.-204+25T>A ENSP00000428884.1:n.-204+25T>A
ENST00000613472.1:c.32-9432T>A ENSP00000480778.1:n.32-9432T>A
NM_003844.3:c.403+25T>A NP_003835.3:n.403+25T>A
NM_003844.4:c.403+25T>A MANE Select NP_003835.3:n.403+25T>A
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