Canonical Allele Identifier: CA1207707981
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1654463184

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173340586G>A , CM000663.2:g.173340586G>A GRCh38
NC_000001.10:g.173309725G>A , CM000663.1:g.173309725G>A GRCh37
NC_000001.9:g.171576348G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037845.1:n.656-100563C>T
XM_017002229.1:c.24+101333C>T XP_016857718.1:n.24+101333C>T
XM_017002230.1:c.18+61673C>T XP_016857719.1:n.18+61673C>T