Canonical Allele Identifier: CA398520245

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1390711436
• gnomAD v3: 17-16948975-T-C
• gnomAD v4: 17-16948975-T-C
• MyVariant Identifiers: chr17:g.16852289T>C (hg19) ; chr17:g.16948975T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948975T>C , CM000679.2:g.16948975T>C	GRCh38
NC_000017.10:g.16852289T>C , CM000679.1:g.16852289T>C	GRCh37
NC_000017.9:g.16793014T>C	NCBI36
NG_007281.1:g.28114A>G , LRG_120:g.28114A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.208A>G MANE Select	ENSP00000261652.2:p.Ser70Gly
ENST00000261652.6:c.208A>G	ENSP00000261652.2:p.Ser70Gly
ENST00000579315.5:c.208A>G	ENSP00000464069.1:p.Ser70Gly
ENST00000581616.2:n.211A>G
ENST00000582931.5:n.112A>G
ENST00000583789.1:c.70A>G	ENSP00000462952.1:p.Ser24Gly
ENST00000584950.5:c.70A>G	ENSP00000463582.1:p.Ser24Gly
NM_012452.2:c.208A>G , LRG_120t1:c.208A>G	NP_036584.1:p.Ser70Gly
NM_012452.3:c.208A>G MANE Select	NP_036584.1:p.Ser70Gly