Canonical Allele Identifier: CA1207707987
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173340605T= , CM000663.2:g.173340605T= GRCh38
NC_000001.10:g.173309744T= , CM000663.1:g.173309744T= GRCh37
NC_000001.9:g.171576367T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037845.1:n.656-100582A=
XM_017002229.1:c.24+101314A= XP_016857718.1:n.24+101314A=
XM_017002230.1:c.18+61654A= XP_016857719.1:n.18+61654A=