Canonical Allele Identifier: CA849990405
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1228175902
MyVariant Identifiers: chr8:g.23069744G>T (hg19) chr8:g.23212231G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212231G>T , CM000670.2:g.23212231G>T GRCh38
NC_000008.10:g.23069744G>T , CM000670.1:g.23069744G>T GRCh37
NC_000008.9:g.23125689G>T NCBI36
NG_032107.1:g.17937C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.307-19C>A MANE Select ENSP00000221132.3:n.307-19C>A
ENST00000221132.7:c.307-19C>A ENSP00000221132.3:n.307-19C>A
ENST00000524158.5:c.-300-19C>A ENSP00000428884.1:n.-300-19C>A
ENST00000613472.1:c.32-9572C>A ENSP00000480778.1:n.32-9572C>A
NM_003844.3:c.307-19C>A NP_003835.3:n.307-19C>A
NM_003844.4:c.307-19C>A MANE Select NP_003835.3:n.307-19C>A
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