Canonical Allele Identifier: CA2636329216
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16948685-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948685C>A , CM000679.2:g.16948685C>A GRCh38
NC_000017.10:g.16851999C>A , CM000679.1:g.16851999C>A GRCh37
NC_000017.9:g.16792724C>A NCBI36
NG_007281.1:g.28404G>T , LRG_120:g.28404G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.445+53G>T MANE Select ENSP00000261652.2:n.445+53G>T
ENST00000261652.6:c.445+53G>T ENSP00000261652.2:n.445+53G>T
ENST00000579315.5:c.445+53G>T ENSP00000464069.1:n.445+53G>T
ENST00000581616.2:n.448+53G>T
ENST00000582931.5:n.349+53G>T
ENST00000583789.1:c.307+53G>T ENSP00000462952.1:n.307+53G>T
ENST00000584950.5:c.307+53G>T ENSP00000463582.1:n.307+53G>T
NM_012452.2:c.445+53G>T , LRG_120t1:c.445+53G>T NP_036584.1:n.445+53G>T
NM_012452.3:c.445+53G>T MANE Select NP_036584.1:n.445+53G>T
Search 100 bp 5'
Search 100 bp 3'