Canonical Allele Identifier: CA625313738

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1484820601
• gnomAD v2: 17-16851984-C-T
• gnomAD v3: 17-16948670-C-T
• gnomAD v4: 17-16948670-C-T
• MyVariant Identifiers: chr17:g.16851984C>T (hg19) ; chr17:g.16948670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948670C>T , CM000679.2:g.16948670C>T	GRCh38
NC_000017.10:g.16851984C>T , CM000679.1:g.16851984C>T	GRCh37
NC_000017.9:g.16792709C>T	NCBI36
NG_007281.1:g.28419G>A , LRG_120:g.28419G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+68G>A MANE Select	ENSP00000261652.2:n.445+68G>A
ENST00000261652.6:c.445+68G>A	ENSP00000261652.2:n.445+68G>A
ENST00000579315.5:c.445+68G>A	ENSP00000464069.1:n.445+68G>A
ENST00000581616.2:n.448+68G>A
ENST00000582931.5:n.349+68G>A
ENST00000583789.1:c.307+68G>A	ENSP00000462952.1:n.307+68G>A
ENST00000584950.5:c.307+68G>A	ENSP00000463582.1:n.307+68G>A
NM_012452.2:c.445+68G>A , LRG_120t1:c.445+68G>A	NP_036584.1:n.445+68G>A
NM_012452.3:c.445+68G>A MANE Select	NP_036584.1:n.445+68G>A