Canonical Allele Identifier: CA398520202

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948956-C-G
• MyVariant Identifiers: chr17:g.16852270C>G (hg19) ; chr17:g.16948956C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948956C>G , CM000679.2:g.16948956C>G	GRCh38
NC_000017.10:g.16852270C>G , CM000679.1:g.16852270C>G	GRCh37
NC_000017.9:g.16792995C>G	NCBI36
NG_007281.1:g.28133G>C , LRG_120:g.28133G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.227G>C MANE Select	ENSP00000261652.2:p.Gly76Ala
ENST00000261652.6:c.227G>C	ENSP00000261652.2:p.Gly76Ala
ENST00000579315.5:c.227G>C	ENSP00000464069.1:p.Gly76Ala
ENST00000581616.2:n.230G>C
ENST00000582931.5:n.131G>C
ENST00000583789.1:c.89G>C	ENSP00000462952.1:p.Gly30Ala
ENST00000584950.5:c.89G>C	ENSP00000463582.1:p.Gly30Ala
NM_012452.2:c.227G>C , LRG_120t1:c.227G>C	NP_036584.1:p.Gly76Ala
NM_012452.3:c.227G>C MANE Select	NP_036584.1:p.Gly76Ala