Canonical Allele Identifier: CA694842505
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1430074308

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267208A>T , CM000675.2:g.108267208A>T GRCh38
NC_000013.10:g.108919556A>T , CM000675.1:g.108919556A>T GRCh37
NC_000013.9:g.107717557A>T NCBI36
NG_029524.1:g.2580A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2892A>T
XR_931715.1:n.1843A>T