Canonical Allele Identifier: CA2250305514

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1196921380

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16949084A>G , CM000679.2:g.16949084A>G	GRCh38
NC_000017.10:g.16852398A>G , CM000679.1:g.16852398A>G	GRCh37
NC_000017.9:g.16793123A>G	NCBI36
NG_007281.1:g.28005T>C , LRG_120:g.28005T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-101T>C MANE Select	ENSP00000261652.2:n.200-101T>C
ENST00000261652.6:c.200-101T>C	ENSP00000261652.2:n.200-101T>C
ENST00000579315.5:c.200-101T>C	ENSP00000464069.1:n.200-101T>C
ENST00000581616.2:n.203-101T>C
ENST00000582931.5:n.104-101T>C
ENST00000583789.1:c.62-101T>C	ENSP00000462952.1:n.62-101T>C
ENST00000584950.5:c.62-101T>C	ENSP00000463582.1:n.62-101T>C
NM_012452.2:c.200-101T>C , LRG_120t1:c.200-101T>C	NP_036584.1:n.200-101T>C
NM_012452.3:c.200-101T>C MANE Select	NP_036584.1:n.200-101T>C