Canonical Allele Identifier: CA398520034
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1008333
ClinVar RCV Id: RCV001305651
dbSNP Id: rs767933010
gnomAD v3: 17-16948879-A-G
gnomAD v4: 17-16948879-A-G
MyVariant Identifiers: chr17:g.16852193A>G (hg19) chr17:g.16948879A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948879A>G , CM000679.2:g.16948879A>G GRCh38
NC_000017.10:g.16852193A>G , CM000679.1:g.16852193A>G GRCh37
NC_000017.9:g.16792918A>G NCBI36
NG_007281.1:g.28210T>C , LRG_120:g.28210T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.304T>C MANE Select ENSP00000261652.2:p.Tyr102His
ENST00000261652.6:c.304T>C ENSP00000261652.2:p.Tyr102His
ENST00000579315.5:c.304T>C ENSP00000464069.1:p.Tyr102His
ENST00000581616.2:n.307T>C
ENST00000582931.5:n.208T>C
ENST00000583789.1:c.166T>C ENSP00000462952.1:p.Tyr56His
ENST00000584950.5:c.166T>C ENSP00000463582.1:p.Tyr56His
NM_012452.2:c.304T>C , LRG_120t1:c.304T>C NP_036584.1:p.Tyr102His
NM_012452.3:c.304T>C MANE Select NP_036584.1:p.Tyr102His
Search 100 bp 5'
Search 100 bp 3'