Canonical Allele Identifier: CA14418266
Gene: TNFRSF13B HGNC NCBI
COSMIC:
COSN6653539 (not active)
MyVariant.info:
GRCh38 chr17:g.16941853A>G
GRCh37 chr17:g.16845167A>G
gnomAD v2:
17:16845167 A / G
gnomAD v3:
17:16941853 A / G
gnomAD v4:
chr17-16941853-A-G
Joint Max Group AF 0.39575192 (EAS)
Genomes Max Group AF 0.39575192 (EAS)
dbSNP:
4792800
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941853A>G , CM000679.2:g.16941853A>G GRCh38
NC_000017.10:g.16845167A>G , CM000679.1:g.16845167A>G GRCh37
NC_000017.9:g.16785892A>G NCBI36
NG_007281.1:g.35236T>C , LRG_120:g.35236T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1342T>C MANE Select ENSP00000261652.2:n.446-1342T>C
ENST00000261652.6:c.446-1342T>C ENSP00000261652.2:n.446-1342T>C
ENST00000579315.5:c.445+6885T>C ENSP00000464069.1:n.445+6885T>C
ENST00000581616.2:n.449-376T>C
ENST00000582931.5:n.349+6885T>C
ENST00000583789.1:c.308-1342T>C ENSP00000462952.1:n.308-1342T>C
ENST00000584950.5:c.308-1342T>C ENSP00000463582.1:n.308-1342T>C
NM_012452.2:c.446-1342T>C , LRG_120t1:c.446-1342T>C NP_036584.1:n.446-1342T>C
NM_012452.3:c.446-1342T>C MANE Select NP_036584.1:n.446-1342T>C
Search 100 bp 5'
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