Canonical Allele Identifier: CA398520025

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852189A>C (hg19) ; chr17:g.16948875A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948875A>C , CM000679.2:g.16948875A>C	GRCh38
NC_000017.10:g.16852189A>C , CM000679.1:g.16852189A>C	GRCh37
NC_000017.9:g.16792914A>C	NCBI36
NG_007281.1:g.28214T>G , LRG_120:g.28214T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.308T>G MANE Select	ENSP00000261652.2:p.Phe103Cys
ENST00000261652.6:c.308T>G	ENSP00000261652.2:p.Phe103Cys
ENST00000579315.5:c.308T>G	ENSP00000464069.1:p.Phe103Cys
ENST00000581616.2:n.311T>G
ENST00000582931.5:n.212T>G
ENST00000583789.1:c.170T>G	ENSP00000462952.1:p.Phe57Cys
ENST00000584950.5:c.170T>G	ENSP00000463582.1:p.Phe57Cys
NM_012452.2:c.308T>G , LRG_120t1:c.308T>G	NP_036584.1:p.Phe103Cys
NM_012452.3:c.308T>G MANE Select	NP_036584.1:p.Phe103Cys