Canonical Allele Identifier: CA288283790
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs556313694
gnomAD v3: 17-16941540-C-G
gnomAD v4: 17-16941540-C-G
MyVariant Identifiers: chr17:g.16844854C>G (hg19) chr17:g.16941540C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941540C>G , CM000679.2:g.16941540C>G GRCh38
NC_000017.10:g.16844854C>G , CM000679.1:g.16844854C>G GRCh37
NC_000017.9:g.16785579C>G NCBI36
NG_007281.1:g.35549G>C , LRG_120:g.35549G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1029G>C MANE Select ENSP00000261652.2:n.446-1029G>C
ENST00000261652.6:c.446-1029G>C ENSP00000261652.2:n.446-1029G>C
ENST00000579315.5:c.445+7198G>C ENSP00000464069.1:n.445+7198G>C
ENST00000581616.2:n.449-63G>C
ENST00000582931.5:n.349+7198G>C
ENST00000583789.1:c.308-1029G>C ENSP00000462952.1:n.308-1029G>C
ENST00000584950.5:c.308-1029G>C ENSP00000463582.1:n.308-1029G>C
NM_012452.2:c.446-1029G>C , LRG_120t1:c.446-1029G>C NP_036584.1:n.446-1029G>C
NM_012452.3:c.446-1029G>C MANE Select NP_036584.1:n.446-1029G>C
Search 100 bp 5'
Search 100 bp 3'