Canonical Allele Identifier: CA624997625
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1306918780
gnomAD v2: 17-16845030-A-G
gnomAD v3: 17-16941716-A-G
gnomAD v4: 17-16941716-A-G
MyVariant Identifiers: chr17:g.16845030A>G (hg19) chr17:g.16941716A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941716A>G , CM000679.2:g.16941716A>G GRCh38
NC_000017.10:g.16845030A>G , CM000679.1:g.16845030A>G GRCh37
NC_000017.9:g.16785755A>G NCBI36
NG_007281.1:g.35373T>C , LRG_120:g.35373T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1205T>C MANE Select ENSP00000261652.2:n.446-1205T>C
ENST00000261652.6:c.446-1205T>C ENSP00000261652.2:n.446-1205T>C
ENST00000579315.5:c.445+7022T>C ENSP00000464069.1:n.445+7022T>C
ENST00000581616.2:n.449-239T>C
ENST00000582931.5:n.349+7022T>C
ENST00000583789.1:c.308-1205T>C ENSP00000462952.1:n.308-1205T>C
ENST00000584950.5:c.308-1205T>C ENSP00000463582.1:n.308-1205T>C
NM_012452.2:c.446-1205T>C , LRG_120t1:c.446-1205T>C NP_036584.1:n.446-1205T>C
NM_012452.3:c.446-1205T>C MANE Select NP_036584.1:n.446-1205T>C
Search 100 bp 5'
Search 100 bp 3'