Canonical Allele Identifier: CA256829082
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs947216782
MyVariant Identifiers: chr13:g.108267220G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267220G>T , CM000675.2:g.108267220G>T GRCh38
NC_000013.10:g.108919568G>T , CM000675.1:g.108919568G>T GRCh37
NC_000013.9:g.107717569G>T NCBI36
NG_029524.1:g.2592G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2880G>T
XR_931715.1:n.1855G>T