Canonical Allele Identifier: CA4674931
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs745812580
ExAC: 8:23069578 G / A
gnomAD v2: 8-23069578-G-A
gnomAD v4: 8-23212065-G-A
MyVariant Identifiers: chr8:g.23069578G>A (hg19) chr8:g.23212065G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212065G>A , CM000670.2:g.23212065G>A GRCh38
NC_000008.10:g.23069578G>A , CM000670.1:g.23069578G>A GRCh37
NC_000008.9:g.23125523G>A NCBI36
NG_032107.1:g.18103C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+51C>T MANE Select ENSP00000221132.3:n.403+51C>T
ENST00000221132.7:c.403+51C>T ENSP00000221132.3:n.403+51C>T
ENST00000524158.5:c.-204+51C>T ENSP00000428884.1:n.-204+51C>T
ENST00000613472.1:c.32-9406C>T ENSP00000480778.1:n.32-9406C>T
NM_003844.3:c.403+51C>T NP_003835.3:n.403+51C>T
NM_003844.4:c.403+51C>T MANE Select NP_003835.3:n.403+51C>T
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