Canonical Allele Identifier: CA8414072

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs758543420
• ExAC: 17:16852293 T / C
• gnomAD v2: 17-16852293-T-C
• gnomAD v4: 17-16948979-T-C
• MyVariant Identifiers: chr17:g.16852293T>C (hg19) ; chr17:g.16948979T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948979T>C , CM000679.2:g.16948979T>C	GRCh38
NC_000017.10:g.16852293T>C , CM000679.1:g.16852293T>C	GRCh37
NC_000017.9:g.16793018T>C	NCBI36
NG_007281.1:g.28110A>G , LRG_120:g.28110A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.204A>G MANE Select	ENSP00000261652.2:p.Ser68=
ENST00000261652.6:c.204A>G	ENSP00000261652.2:p.Ser68=
ENST00000579315.5:c.204A>G	ENSP00000464069.1:p.Ser68=
ENST00000581616.2:n.207A>G
ENST00000582931.5:n.108A>G
ENST00000583789.1:c.66A>G	ENSP00000462952.1:p.Ser22=
ENST00000584950.5:c.66A>G	ENSP00000463582.1:p.Ser22=
NM_012452.2:c.204A>G , LRG_120t1:c.204A>G	NP_036584.1:p.Ser68=
NM_012452.3:c.204A>G MANE Select	NP_036584.1:p.Ser68=