Canonical Allele Identifier: CA2250341620
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs2087749592
gnomAD v4: 17-16972090-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16972090A>G , CM000679.2:g.16972090A>G GRCh38
NC_000017.10:g.16875404A>G , CM000679.1:g.16875404A>G GRCh37
NC_000017.9:g.16816129A>G NCBI36
NG_007281.1:g.4999T>C , LRG_120:g.4999T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.-15T>C MANE Select ENSP00000261652.2:n.-15T>C
ENST00000579315.5:c.-15T>C ENSP00000464069.1:n.-15T>C
ENST00000582931.5:n.28T>C
NM_012452.3:c.-15T>C MANE Select NP_036584.1:n.-15T>C
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