Canonical Allele Identifier: CA173948521
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs148868243
COSMIC: COSM107530
MyVariant Identifiers: chr8:g.23069654G>A (hg19) chr8:g.23212141G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212141G>A , CM000670.2:g.23212141G>A GRCh38
NC_000008.10:g.23069654G>A , CM000670.1:g.23069654G>A GRCh37
NC_000008.9:g.23125599G>A NCBI36
NG_032107.1:g.18027C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.378C>T MANE Select ENSP00000221132.3:p.Ser126=
ENST00000221132.7:c.378C>T ENSP00000221132.3:p.Ser126=
ENST00000524158.5:c.-229C>T ENSP00000428884.1:n.-229C>T
ENST00000613472.1:c.32-9482C>T ENSP00000480778.1:n.32-9482C>T
NM_003844.3:c.378C>T NP_003835.3:p.Ser126=
NM_003844.4:c.378C>T MANE Select NP_003835.3:p.Ser126=
Search 100 bp 5'
Search 100 bp 3'