Canonical Allele Identifier: CA398520250

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852292G>C (hg19) ; chr17:g.16948978G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948978G>C , CM000679.2:g.16948978G>C	GRCh38
NC_000017.10:g.16852292G>C , CM000679.1:g.16852292G>C	GRCh37
NC_000017.9:g.16793017G>C	NCBI36
NG_007281.1:g.28111C>G , LRG_120:g.28111C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.205C>G MANE Select	ENSP00000261652.2:p.Leu69Val
ENST00000261652.6:c.205C>G	ENSP00000261652.2:p.Leu69Val
ENST00000579315.5:c.205C>G	ENSP00000464069.1:p.Leu69Val
ENST00000581616.2:n.208C>G
ENST00000582931.5:n.109C>G
ENST00000583789.1:c.67C>G	ENSP00000462952.1:p.Leu23Val
ENST00000584950.5:c.67C>G	ENSP00000463582.1:p.Leu23Val
NM_012452.2:c.205C>G , LRG_120t1:c.205C>G	NP_036584.1:p.Leu69Val
NM_012452.3:c.205C>G MANE Select	NP_036584.1:p.Leu69Val