Canonical Allele Identifier: CA2636329194
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16948658-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948658C>T , CM000679.2:g.16948658C>T GRCh38
NC_000017.10:g.16851972C>T , CM000679.1:g.16851972C>T GRCh37
NC_000017.9:g.16792697C>T NCBI36
NG_007281.1:g.28431G>A , LRG_120:g.28431G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.445+80G>A MANE Select ENSP00000261652.2:n.445+80G>A
ENST00000261652.6:c.445+80G>A ENSP00000261652.2:n.445+80G>A
ENST00000579315.5:c.445+80G>A ENSP00000464069.1:n.445+80G>A
ENST00000581616.2:n.448+80G>A
ENST00000582931.5:n.349+80G>A
ENST00000583789.1:c.307+80G>A ENSP00000462952.1:n.307+80G>A
ENST00000584950.5:c.307+80G>A ENSP00000463582.1:n.307+80G>A
NM_012452.2:c.445+80G>A , LRG_120t1:c.445+80G>A NP_036584.1:n.445+80G>A
NM_012452.3:c.445+80G>A MANE Select NP_036584.1:n.445+80G>A
Search 100 bp 5'
Search 100 bp 3'