Canonical Allele Identifier: CA1009231238
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1342038

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173332377G>C , CM000663.2:g.173332377G>C GRCh38
NC_000001.10:g.173301516G>C , CM000663.1:g.173301516G>C GRCh37
NC_000001.9:g.171568139G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037845.1:n.656-92354C>G
XM_017002229.1:c.24+109542C>G XP_016857718.1:n.24+109542C>G
XM_017002230.1:c.18+69882C>G XP_016857719.1:n.18+69882C>G