Canonical Allele Identifier: CA624997584
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1282869745
gnomAD v2: 17-16844841-G-C
gnomAD v3: 17-16941527-G-C
gnomAD v4: 17-16941527-G-C
MyVariant Identifiers: chr17:g.16844841G>C (hg19) chr17:g.16941527G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941527G>C , CM000679.2:g.16941527G>C GRCh38
NC_000017.10:g.16844841G>C , CM000679.1:g.16844841G>C GRCh37
NC_000017.9:g.16785566G>C NCBI36
NG_007281.1:g.35562C>G , LRG_120:g.35562C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1016C>G MANE Select ENSP00000261652.2:n.446-1016C>G
ENST00000261652.6:c.446-1016C>G ENSP00000261652.2:n.446-1016C>G
ENST00000579315.5:c.445+7211C>G ENSP00000464069.1:n.445+7211C>G
ENST00000581616.2:n.449-50C>G
ENST00000582931.5:n.349+7211C>G
ENST00000583789.1:c.308-1016C>G ENSP00000462952.1:n.308-1016C>G
ENST00000584950.5:c.308-1016C>G ENSP00000463582.1:n.308-1016C>G
NM_012452.2:c.446-1016C>G , LRG_120t1:c.446-1016C>G NP_036584.1:n.446-1016C>G
NM_012452.3:c.446-1016C>G MANE Select NP_036584.1:n.446-1016C>G
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