Canonical Allele Identifier: CA8413992

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs780316609
• ExAC: 17:16852001 A / G
• gnomAD v2: 17-16852001-A-G
• gnomAD v4: 17-16948687-A-G
• MyVariant Identifiers: chr17:g.16852001A>G (hg19) ; chr17:g.16948687A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948687A>G , CM000679.2:g.16948687A>G	GRCh38
NC_000017.10:g.16852001A>G , CM000679.1:g.16852001A>G	GRCh37
NC_000017.9:g.16792726A>G	NCBI36
NG_007281.1:g.28402T>C , LRG_120:g.28402T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+51T>C MANE Select	ENSP00000261652.2:n.445+51T>C
ENST00000261652.6:c.445+51T>C	ENSP00000261652.2:n.445+51T>C
ENST00000579315.5:c.445+51T>C	ENSP00000464069.1:n.445+51T>C
ENST00000581616.2:n.448+51T>C
ENST00000582931.5:n.349+51T>C
ENST00000583789.1:c.307+51T>C	ENSP00000462952.1:n.307+51T>C
ENST00000584950.5:c.307+51T>C	ENSP00000463582.1:n.307+51T>C
NM_012452.2:c.445+51T>C , LRG_120t1:c.445+51T>C	NP_036584.1:n.445+51T>C
NM_012452.3:c.445+51T>C MANE Select	NP_036584.1:n.445+51T>C