Canonical Allele Identifier: CA2250293037
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs2087513022
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941866T>C , CM000679.2:g.16941866T>C GRCh38
NC_000017.10:g.16845180T>C , CM000679.1:g.16845180T>C GRCh37
NC_000017.9:g.16785905T>C NCBI36
NG_007281.1:g.35223A>G , LRG_120:g.35223A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.446-1355A>G MANE Select ENSP00000261652.2:n.446-1355A>G
ENST00000261652.6:c.446-1355A>G ENSP00000261652.2:n.446-1355A>G
ENST00000579315.5:c.445+6872A>G ENSP00000464069.1:n.445+6872A>G
ENST00000581616.2:n.449-389A>G
ENST00000582931.5:n.349+6872A>G
ENST00000583789.1:c.308-1355A>G ENSP00000462952.1:n.308-1355A>G
ENST00000584950.5:c.308-1355A>G ENSP00000463582.1:n.308-1355A>G
NM_012452.2:c.446-1355A>G , LRG_120t1:c.446-1355A>G NP_036584.1:n.446-1355A>G
NM_012452.3:c.446-1355A>G MANE Select NP_036584.1:n.446-1355A>G
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