Canonical Allele Identifier: CA2250292745

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs2087511111

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941660A>G , CM000679.2:g.16941660A>G	GRCh38
NC_000017.10:g.16844974A>G , CM000679.1:g.16844974A>G	GRCh37
NC_000017.9:g.16785699A>G	NCBI36
NG_007281.1:g.35429T>C , LRG_120:g.35429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1149T>C MANE Select	ENSP00000261652.2:n.446-1149T>C
ENST00000261652.6:c.446-1149T>C	ENSP00000261652.2:n.446-1149T>C
ENST00000579315.5:c.445+7078T>C	ENSP00000464069.1:n.445+7078T>C
ENST00000581616.2:n.449-183T>C
ENST00000582931.5:n.349+7078T>C
ENST00000583789.1:c.308-1149T>C	ENSP00000462952.1:n.308-1149T>C
ENST00000584950.5:c.308-1149T>C	ENSP00000463582.1:n.308-1149T>C
NM_012452.2:c.446-1149T>C , LRG_120t1:c.446-1149T>C	NP_036584.1:n.446-1149T>C
NM_012452.3:c.446-1149T>C MANE Select	NP_036584.1:n.446-1149T>C