Canonical Allele Identifier: CA10692079

Gene: TNFSF4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173208253C>G , CM000663.2:g.173208253C>G	GRCh38
NC_000001.10:g.173177392C>G , CM000663.1:g.173177392C>G	GRCh37
NC_000001.9:g.171444015C>G	NCBI36
NG_011477.1:g.4080G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011509964.2:c.-9G>C	XP_011508266.2:n.-9G>C
XM_017002229.1:c.25-1068G>C	XP_016857718.1:n.25-1068G>C
XM_017002230.1:c.19-1068G>C	XP_016857719.1:n.19-1068G>C