Canonical Allele Identifier: CA4674932
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs771985462
ExAC: 8:23069584 G / T
gnomAD v2: 8-23069584-G-T
gnomAD v4: 8-23212071-G-T
MyVariant Identifiers: chr8:g.23069584G>T (hg19) chr8:g.23212071G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212071G>T , CM000670.2:g.23212071G>T GRCh38
NC_000008.10:g.23069584G>T , CM000670.1:g.23069584G>T GRCh37
NC_000008.9:g.23125529G>T NCBI36
NG_032107.1:g.18097C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+45C>A MANE Select ENSP00000221132.3:n.403+45C>A
ENST00000221132.7:c.403+45C>A ENSP00000221132.3:n.403+45C>A
ENST00000524158.5:c.-204+45C>A ENSP00000428884.1:n.-204+45C>A
ENST00000613472.1:c.32-9412C>A ENSP00000480778.1:n.32-9412C>A
NM_003844.3:c.403+45C>A NP_003835.3:n.403+45C>A
NM_003844.4:c.403+45C>A MANE Select NP_003835.3:n.403+45C>A
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