Canonical Allele Identifier: CA498106028

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16875378C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16972064C>G , CM000679.2:g.16972064C>G	GRCh38
NC_000017.10:g.16875378C>G , CM000679.1:g.16875378C>G	GRCh37
NC_000017.9:g.16816103C>G	NCBI36
NG_007281.1:g.5025G>C , LRG_120:g.5025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.12G>C MANE Select	ENSP00000261652.2:p.Leu4=
ENST00000261652.6:c.12G>C	ENSP00000261652.2:p.Leu4=
ENST00000579315.5:c.12G>C	ENSP00000464069.1:p.Leu4=
ENST00000581616.2:n.15G>C
ENST00000582931.5:n.54G>C
ENST00000583789.1:c.12G>C	ENSP00000462952.1:p.Leu4=
ENST00000584950.5:c.12G>C	ENSP00000463582.1:p.Leu4=
NM_012452.2:c.12G>C , LRG_120t1:c.12G>C	NP_036584.1:p.Leu4=
NM_012452.3:c.12G>C MANE Select	NP_036584.1:p.Leu4=