Canonical Allele Identifier: CA2636331914
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16972112-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16972113del , CM000679.2:g.16972113del GRCh38
NC_000017.10:g.16875427del , CM000679.1:g.16875427del GRCh37
NC_000017.9:g.16816152del NCBI36
NG_007281.1:g.4976del , LRG_120:g.4976del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.-38del MANE Select ENSP00000261652.2:n.-38del
ENST00000579315.5:c.-38del ENSP00000464069.1:n.-38del
ENST00000582931.5:n.5del
NM_012452.3:c.-38del MANE Select NP_036584.1:n.-38del
Search 100 bp 5'
Search 100 bp 3'