Canonical Allele Identifier: CA624997599
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1429546062
gnomAD v2: 17-16844886-C-T
gnomAD v3: 17-16941572-C-T
gnomAD v4: 17-16941572-C-T
MyVariant Identifiers: chr17:g.16844886C>T (hg19) chr17:g.16941572C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941572C>T , CM000679.2:g.16941572C>T GRCh38
NC_000017.10:g.16844886C>T , CM000679.1:g.16844886C>T GRCh37
NC_000017.9:g.16785611C>T NCBI36
NG_007281.1:g.35517G>A , LRG_120:g.35517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1061G>A MANE Select ENSP00000261652.2:n.446-1061G>A
ENST00000261652.6:c.446-1061G>A ENSP00000261652.2:n.446-1061G>A
ENST00000579315.5:c.445+7166G>A ENSP00000464069.1:n.445+7166G>A
ENST00000581616.2:n.449-95G>A
ENST00000582931.5:n.349+7166G>A
ENST00000583789.1:c.308-1061G>A ENSP00000462952.1:n.308-1061G>A
ENST00000584950.5:c.308-1061G>A ENSP00000463582.1:n.308-1061G>A
NM_012452.2:c.446-1061G>A , LRG_120t1:c.446-1061G>A NP_036584.1:n.446-1061G>A
NM_012452.3:c.446-1061G>A MANE Select NP_036584.1:n.446-1061G>A
Search 100 bp 5'
Search 100 bp 3'