Canonical Allele Identifier: CA10639005
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 322028
ClinVar RCV Id: RCV000323777 RCV002521095
dbSNP Id: rs886052653
gnomAD v4: 17-16948982-C-G
MyVariant Identifiers: chr17:g.16852296C>G (hg19) chr17:g.16948982C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948982C>G , CM000679.2:g.16948982C>G GRCh38
NC_000017.10:g.16852296C>G , CM000679.1:g.16852296C>G GRCh37
NC_000017.9:g.16793021C>G NCBI36
NG_007281.1:g.28107G>C , LRG_120:g.28107G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.201G>C MANE Select ENSP00000261652.2:p.Arg67Ser
ENST00000261652.6:c.201G>C ENSP00000261652.2:p.Arg67Ser
ENST00000579315.5:c.201G>C ENSP00000464069.1:p.Arg67Ser
ENST00000581616.2:n.204G>C
ENST00000582931.5:n.105G>C
ENST00000583789.1:c.63G>C ENSP00000462952.1:p.Trp21Cys
ENST00000584950.5:c.63G>C ENSP00000463582.1:p.Trp21Cys
NM_012452.2:c.201G>C , LRG_120t1:c.201G>C NP_036584.1:p.Arg67Ser
NM_012452.3:c.201G>C MANE Select NP_036584.1:p.Arg67Ser
Search 100 bp 5'
Search 100 bp 3'