Canonical Allele Identifier: CA33051386
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs373925009
gnomAD v2: 1-173309749-G-A
gnomAD v3: 1-173340610-G-A
gnomAD v4: 1-173340610-G-A
MyVariant Identifiers: chr1:g.173309749G>A (hg19) chr1:g.173340610G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173340610G>A , CM000663.2:g.173340610G>A GRCh38
NC_000001.10:g.173309749G>A , CM000663.1:g.173309749G>A GRCh37
NC_000001.9:g.171576372G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037845.1:n.656-100587C>T
XM_017002229.1:c.24+101309C>T XP_016857718.1:n.24+101309C>T
XM_017002230.1:c.18+61649C>T XP_016857719.1:n.18+61649C>T
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