Canonical Allele Identifier: CA849995859
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1348211898
gnomAD v3: 8-23222613-G-A
gnomAD v4: 8-23222613-G-A
MyVariant Identifiers: chr8:g.23080126G>A (hg19) chr8:g.23222613G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222613G>A , CM000670.2:g.23222613G>A GRCh38
NC_000008.10:g.23080126G>A , CM000670.1:g.23080126G>A GRCh37
NC_000008.9:g.23136071G>A NCBI36
NG_032107.1:g.7555C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2143C>T MANE Select ENSP00000221132.3:n.306+2143C>T
ENST00000221132.7:c.306+2143C>T ENSP00000221132.3:n.306+2143C>T
ENST00000524158.5:c.-301+1820C>T ENSP00000428884.1:n.-301+1820C>T
ENST00000613472.1:c.31+2418C>T ENSP00000480778.1:n.31+2418C>T
NM_003844.3:c.306+2143C>T NP_003835.3:n.306+2143C>T
NM_003844.4:c.306+2143C>T MANE Select NP_003835.3:n.306+2143C>T
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