Canonical Allele Identifier: CA398520075
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948898C>A , CM000679.2:g.16948898C>A GRCh38
NC_000017.10:g.16852212C>A , CM000679.1:g.16852212C>A GRCh37
NC_000017.9:g.16792937C>A NCBI36
NG_007281.1:g.28191G>T , LRG_120:g.28191G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.285G>T MANE Select ENSP00000261652.2:p.Gln95His
ENST00000261652.6:c.285G>T ENSP00000261652.2:p.Gln95His
ENST00000579315.5:c.285G>T ENSP00000464069.1:p.Gln95His
ENST00000581616.2:n.288G>T
ENST00000582931.5:n.189G>T
ENST00000583789.1:c.147G>T ENSP00000462952.1:p.Gln49His
ENST00000584950.5:c.147G>T ENSP00000463582.1:p.Gln49His
NM_012452.2:c.285G>T , LRG_120t1:c.285G>T NP_036584.1:p.Gln95His
NM_012452.3:c.285G>T MANE Select NP_036584.1:p.Gln95His