Canonical Allele Identifier: CA398519858

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948797-T-C
• MyVariant Identifiers: chr17:g.16852111T>C (hg19) ; chr17:g.16948797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948797T>C , CM000679.2:g.16948797T>C	GRCh38
NC_000017.10:g.16852111T>C , CM000679.1:g.16852111T>C	GRCh37
NC_000017.9:g.16792836T>C	NCBI36
NG_007281.1:g.28292A>G , LRG_120:g.28292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.386A>G MANE Select	ENSP00000261652.2:p.Asn129Ser
ENST00000261652.6:c.386A>G	ENSP00000261652.2:p.Asn129Ser
ENST00000579315.5:c.386A>G	ENSP00000464069.1:p.Asn129Ser
ENST00000581616.2:n.389A>G
ENST00000582931.5:n.290A>G
ENST00000583789.1:c.248A>G	ENSP00000462952.1:p.Asn83Ser
ENST00000584950.5:c.248A>G	ENSP00000463582.1:p.Asn83Ser
NM_012452.2:c.386A>G , LRG_120t1:c.386A>G	NP_036584.1:p.Asn129Ser
NM_012452.3:c.386A>G MANE Select	NP_036584.1:p.Asn129Ser