Canonical Allele Identifier: CA498420120

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852068G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948754G>C , CM000679.2:g.16948754G>C	GRCh38
NC_000017.10:g.16852068G>C , CM000679.1:g.16852068G>C	GRCh37
NC_000017.9:g.16792793G>C	NCBI36
NG_007281.1:g.28335C>G , LRG_120:g.28335C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.429C>G MANE Select	ENSP00000261652.2:p.Gly143=
ENST00000261652.6:c.429C>G	ENSP00000261652.2:p.Gly143=
ENST00000579315.5:c.429C>G	ENSP00000464069.1:p.Gly143=
ENST00000581616.2:n.432C>G
ENST00000582931.5:n.333C>G
ENST00000583789.1:c.291C>G	ENSP00000462952.1:p.Gly97=
ENST00000584950.5:c.291C>G	ENSP00000463582.1:p.Gly97=
NM_012452.2:c.429C>G , LRG_120t1:c.429C>G	NP_036584.1:p.Gly143=
NM_012452.3:c.429C>G MANE Select	NP_036584.1:p.Gly143=