Canonical Allele Identifier: CA10692079
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1234314

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