Canonical Allele Identifier: CA398520668
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16972062C>T , CM000679.2:g.16972062C>T GRCh38
NC_000017.10:g.16875376C>T , CM000679.1:g.16875376C>T GRCh37
NC_000017.9:g.16816101C>T NCBI36
NG_007281.1:g.5027G>A , LRG_120:g.5027G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.14G>A MANE Select ENSP00000261652.2:p.Gly5Asp
ENST00000261652.6:c.14G>A ENSP00000261652.2:p.Gly5Asp
ENST00000579315.5:c.14G>A ENSP00000464069.1:p.Gly5Asp
ENST00000581616.2:n.17G>A
ENST00000582931.5:n.56G>A
ENST00000583789.1:c.14G>A ENSP00000462952.1:p.Gly5Asp
ENST00000584950.5:c.14G>A ENSP00000463582.1:p.Gly5Asp
NM_012452.2:c.14G>A , LRG_120t1:c.14G>A NP_036584.1:p.Gly5Asp
NM_012452.3:c.14G>A MANE Select NP_036584.1:p.Gly5Asp