Canonical Allele Identifier: CA370583122
Gene: TNFRSF10A HGNC NCBI

Linked Data

gnomAD v4: 8-23212125-A-G
MyVariant Identifiers: chr8:g.23069638A>G (hg19) chr8:g.23212125A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212125A>G , CM000670.2:g.23212125A>G GRCh38
NC_000008.10:g.23069638A>G , CM000670.1:g.23069638A>G GRCh37
NC_000008.9:g.23125583A>G NCBI36
NG_032107.1:g.18043T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.394T>C MANE Select ENSP00000221132.3:p.Cys132Arg
ENST00000221132.7:c.394T>C ENSP00000221132.3:p.Cys132Arg
ENST00000524158.5:c.-213T>C ENSP00000428884.1:n.-213T>C
ENST00000613472.1:c.32-9466T>C ENSP00000480778.1:n.32-9466T>C
NM_003844.3:c.394T>C NP_003835.3:p.Cys132Arg
NM_003844.4:c.394T>C MANE Select NP_003835.3:p.Cys132Arg
Search 100 bp 5'
Search 100 bp 3'