Canonical Allele Identifier: CA1207707996
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1571291093

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173340643A>C , CM000663.2:g.173340643A>C GRCh38
NC_000001.10:g.173309782A>C , CM000663.1:g.173309782A>C GRCh37
NC_000001.9:g.171576405A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037845.1:n.656-100620T>G
XM_017002229.1:c.24+101276T>G XP_016857718.1:n.24+101276T>G
XM_017002230.1:c.18+61616T>G XP_016857719.1:n.18+61616T>G