Canonical Allele Identifier: CA2250305302
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2830825
ClinVar RCV Id: RCV003613920
dbSNP Id: rs1229410555
gnomAD v4: 17-16948990-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948990G>T , CM000679.2:g.16948990G>T GRCh38
NC_000017.10:g.16852304G>T , CM000679.1:g.16852304G>T GRCh37
NC_000017.9:g.16793029G>T NCBI36
NG_007281.1:g.28099C>A , LRG_120:g.28099C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.200-7C>A MANE Select ENSP00000261652.2:n.200-7C>A
ENST00000261652.6:c.200-7C>A ENSP00000261652.2:n.200-7C>A
ENST00000579315.5:c.200-7C>A ENSP00000464069.1:n.200-7C>A
ENST00000581616.2:n.203-7C>A
ENST00000582931.5:n.104-7C>A
ENST00000583789.1:c.62-7C>A ENSP00000462952.1:n.62-7C>A
ENST00000584950.5:c.62-7C>A ENSP00000463582.1:n.62-7C>A
NM_012452.2:c.200-7C>A , LRG_120t1:c.200-7C>A NP_036584.1:n.200-7C>A
NM_012452.3:c.200-7C>A MANE Select NP_036584.1:n.200-7C>A
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