Canonical Allele Identifier: CA398519995
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948862C>G , CM000679.2:g.16948862C>G GRCh38
NC_000017.10:g.16852176C>G , CM000679.1:g.16852176C>G GRCh37
NC_000017.9:g.16792901C>G NCBI36
NG_007281.1:g.28227G>C , LRG_120:g.28227G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.321G>C MANE Select ENSP00000261652.2:p.Lys107Asn
ENST00000261652.6:c.321G>C ENSP00000261652.2:p.Lys107Asn
ENST00000579315.5:c.321G>C ENSP00000464069.1:p.Lys107Asn
ENST00000581616.2:n.324G>C
ENST00000582931.5:n.225G>C
ENST00000583789.1:c.183G>C ENSP00000462952.1:p.Lys61Asn
ENST00000584950.5:c.183G>C ENSP00000463582.1:p.Lys61Asn
NM_012452.2:c.321G>C , LRG_120t1:c.321G>C NP_036584.1:p.Lys107Asn
NM_012452.3:c.321G>C MANE Select NP_036584.1:p.Lys107Asn