Canonical Allele Identifier: CA398519772

Gene: TNFRSF13B

Linked Data

• ClinVar Variation Id: 2115609
• ClinVar RCV Id: RCV003032745
• MyVariant Identifiers: chr17:g.16852072C>G (hg19) ; chr17:g.16948758C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948758C>G , CM000679.2:g.16948758C>G	GRCh38
NC_000017.10:g.16852072C>G , CM000679.1:g.16852072C>G	GRCh37
NC_000017.9:g.16792797C>G	NCBI36
NG_007281.1:g.28331G>C , LRG_120:g.28331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.425G>C MANE Select	ENSP00000261652.2:p.Arg142Thr
ENST00000261652.6:c.425G>C	ENSP00000261652.2:p.Arg142Thr
ENST00000579315.5:c.425G>C	ENSP00000464069.1:p.Arg142Thr
ENST00000581616.2:n.428G>C
ENST00000582931.5:n.329G>C
ENST00000583789.1:c.287G>C	ENSP00000462952.1:p.Arg96Thr
ENST00000584950.5:c.287G>C	ENSP00000463582.1:p.Arg96Thr
NM_012452.2:c.425G>C , LRG_120t1:c.425G>C	NP_036584.1:p.Arg142Thr
NM_012452.3:c.425G>C MANE Select	NP_036584.1:p.Arg142Thr