Canonical Allele Identifier: CA398520261
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948983C>T , CM000679.2:g.16948983C>T GRCh38
NC_000017.10:g.16852297C>T , CM000679.1:g.16852297C>T GRCh37
NC_000017.9:g.16793022C>T NCBI36
NG_007281.1:g.28106G>A , LRG_120:g.28106G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.200G>A MANE Select ENSP00000261652.2:p.Arg67Lys
ENST00000261652.6:c.200G>A ENSP00000261652.2:p.Arg67Lys
ENST00000579315.5:c.200G>A ENSP00000464069.1:p.Arg67Lys
ENST00000581616.2:n.203G>A
ENST00000582931.5:n.104G>A
ENST00000583789.1:c.62G>A ENSP00000462952.1:p.Trp21Ter
ENST00000584950.5:c.62G>A ENSP00000463582.1:p.Trp21Ter
NM_012452.2:c.200G>A , LRG_120t1:c.200G>A NP_036584.1:p.Arg67Lys
NM_012452.3:c.200G>A MANE Select NP_036584.1:p.Arg67Lys