Canonical Allele Identifier: CA398520128

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948923-A-G
• MyVariant Identifiers: chr17:g.16852237A>G (hg19) ; chr17:g.16948923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948923A>G , CM000679.2:g.16948923A>G	GRCh38
NC_000017.10:g.16852237A>G , CM000679.1:g.16852237A>G	GRCh37
NC_000017.9:g.16792962A>G	NCBI36
NG_007281.1:g.28166T>C , LRG_120:g.28166T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.260T>C MANE Select	ENSP00000261652.2:p.Ile87Thr
ENST00000261652.6:c.260T>C	ENSP00000261652.2:p.Ile87Thr
ENST00000579315.5:c.260T>C	ENSP00000464069.1:p.Ile87Thr
ENST00000581616.2:n.263T>C
ENST00000582931.5:n.164T>C
ENST00000583789.1:c.122T>C	ENSP00000462952.1:p.Ile41Thr
ENST00000584950.5:c.122T>C	ENSP00000463582.1:p.Ile41Thr
NM_012452.2:c.260T>C , LRG_120t1:c.260T>C	NP_036584.1:p.Ile87Thr
NM_012452.3:c.260T>C MANE Select	NP_036584.1:p.Ile87Thr