Canonical Allele Identifier: CA2576183857
Gene: TNFRSF13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948659C>T , CM000679.2:g.16948659C>T GRCh38
NC_000017.10:g.16851973C>T , CM000679.1:g.16851973C>T GRCh37
NC_000017.9:g.16792698C>T NCBI36
NG_007281.1:g.28430G>A , LRG_120:g.28430G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.445+79G>A MANE Select ENSP00000261652.2:n.445+79G>A
ENST00000261652.6:c.445+79G>A ENSP00000261652.2:n.445+79G>A
ENST00000579315.5:c.445+79G>A ENSP00000464069.1:n.445+79G>A
ENST00000581616.2:n.448+79G>A
ENST00000582931.5:n.349+79G>A
ENST00000583789.1:c.307+79G>A ENSP00000462952.1:n.307+79G>A
ENST00000584950.5:c.307+79G>A ENSP00000463582.1:n.307+79G>A
NM_012452.2:c.445+79G>A , LRG_120t1:c.445+79G>A NP_036584.1:n.445+79G>A
NM_012452.3:c.445+79G>A MANE Select NP_036584.1:n.445+79G>A
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Search 100 bp 3'