Canonical Allele Identifier: CA4674933
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs200864314
ExAC: 8:23069590 G / C
gnomAD v2: 8-23069590-G-C
gnomAD v3: 8-23212077-G-C
gnomAD v4: 8-23212077-G-C
MyVariant Identifiers: chr8:g.23069590G>C (hg19) chr8:g.23212077G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212077G>C , CM000670.2:g.23212077G>C GRCh38
NC_000008.10:g.23069590G>C , CM000670.1:g.23069590G>C GRCh37
NC_000008.9:g.23125535G>C NCBI36
NG_032107.1:g.18091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+39C>G MANE Select ENSP00000221132.3:n.403+39C>G
ENST00000221132.7:c.403+39C>G ENSP00000221132.3:n.403+39C>G
ENST00000524158.5:c.-204+39C>G ENSP00000428884.1:n.-204+39C>G
ENST00000613472.1:c.32-9418C>G ENSP00000480778.1:n.32-9418C>G
NM_003844.3:c.403+39C>G NP_003835.3:n.403+39C>G
NM_003844.4:c.403+39C>G MANE Select NP_003835.3:n.403+39C>G
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