Canonical Allele Identifier: CA370583137
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1169750241
gnomAD v3: 8-23212131-C-G
gnomAD v4: 8-23212131-C-G
MyVariant Identifiers: chr8:g.23069644C>G (hg19) chr8:g.23212131C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212131C>G , CM000670.2:g.23212131C>G GRCh38
NC_000008.10:g.23069644C>G , CM000670.1:g.23069644C>G GRCh37
NC_000008.9:g.23125589C>G NCBI36
NG_032107.1:g.18037G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.388G>C MANE Select ENSP00000221132.3:p.Glu130Gln
ENST00000221132.7:c.388G>C ENSP00000221132.3:p.Glu130Gln
ENST00000524158.5:c.-219G>C ENSP00000428884.1:n.-219G>C
ENST00000613472.1:c.32-9472G>C ENSP00000480778.1:n.32-9472G>C
NM_003844.3:c.388G>C NP_003835.3:p.Glu130Gln
NM_003844.4:c.388G>C MANE Select NP_003835.3:p.Glu130Gln
Search 100 bp 5'
Search 100 bp 3'