Canonical Allele Identifier: CA624997628
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1357093993
gnomAD v2: 17-16845045-C-G
gnomAD v3: 17-16941731-C-G
gnomAD v4: 17-16941731-C-G
MyVariant Identifiers: chr17:g.16845045C>G (hg19) chr17:g.16941731C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941731C>G , CM000679.2:g.16941731C>G GRCh38
NC_000017.10:g.16845045C>G , CM000679.1:g.16845045C>G GRCh37
NC_000017.9:g.16785770C>G NCBI36
NG_007281.1:g.35358G>C , LRG_120:g.35358G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1220G>C MANE Select ENSP00000261652.2:n.446-1220G>C
ENST00000261652.6:c.446-1220G>C ENSP00000261652.2:n.446-1220G>C
ENST00000579315.5:c.445+7007G>C ENSP00000464069.1:n.445+7007G>C
ENST00000581616.2:n.449-254G>C
ENST00000582931.5:n.349+7007G>C
ENST00000583789.1:c.308-1220G>C ENSP00000462952.1:n.308-1220G>C
ENST00000584950.5:c.308-1220G>C ENSP00000463582.1:n.308-1220G>C
NM_012452.2:c.446-1220G>C , LRG_120t1:c.446-1220G>C NP_036584.1:n.446-1220G>C
NM_012452.3:c.446-1220G>C MANE Select NP_036584.1:n.446-1220G>C
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