Canonical Allele Identifier: CA398520635
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16972044C>G , CM000679.2:g.16972044C>G GRCh38
NC_000017.10:g.16875358C>G , CM000679.1:g.16875358C>G GRCh37
NC_000017.9:g.16816083C>G NCBI36
NG_007281.1:g.5045G>C , LRG_120:g.5045G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.32G>C MANE Select ENSP00000261652.2:p.Gly11Ala
ENST00000261652.6:c.32G>C ENSP00000261652.2:p.Gly11Ala
ENST00000579315.5:c.32G>C ENSP00000464069.1:p.Gly11Ala
ENST00000581616.2:n.35G>C
ENST00000582931.5:n.74G>C
ENST00000583789.1:c.32G>C ENSP00000462952.1:p.Gly11Ala
ENST00000584950.5:c.32G>C ENSP00000463582.1:p.Gly11Ala
NM_012452.2:c.32G>C , LRG_120t1:c.32G>C NP_036584.1:p.Gly11Ala
NM_012452.3:c.32G>C MANE Select NP_036584.1:p.Gly11Ala