Canonical Allele Identifier: CA1770800780
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1801272883
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222677C>A , CM000670.2:g.23222677C>A GRCh38
NC_000008.10:g.23080190C>A , CM000670.1:g.23080190C>A GRCh37
NC_000008.9:g.23136135C>A NCBI36
NG_032107.1:g.7491G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2079G>T MANE Select ENSP00000221132.3:n.306+2079G>T
ENST00000221132.7:c.306+2079G>T ENSP00000221132.3:n.306+2079G>T
ENST00000524158.5:c.-301+1756G>T ENSP00000428884.1:n.-301+1756G>T
ENST00000613472.1:c.31+2354G>T ENSP00000480778.1:n.31+2354G>T
NM_003844.3:c.306+2079G>T NP_003835.3:n.306+2079G>T
NM_003844.4:c.306+2079G>T MANE Select NP_003835.3:n.306+2079G>T
Search 100 bp 5'
Search 100 bp 3'