Canonical Allele Identifier: CA498420127

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852074G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948760G>A , CM000679.2:g.16948760G>A	GRCh38
NC_000017.10:g.16852074G>A , CM000679.1:g.16852074G>A	GRCh37
NC_000017.9:g.16792799G>A	NCBI36
NG_007281.1:g.28329C>T , LRG_120:g.28329C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.423C>T MANE Select	ENSP00000261652.2:p.His141=
ENST00000261652.6:c.423C>T	ENSP00000261652.2:p.His141=
ENST00000579315.5:c.423C>T	ENSP00000464069.1:p.His141=
ENST00000581616.2:n.426C>T
ENST00000582931.5:n.327C>T
ENST00000583789.1:c.285C>T	ENSP00000462952.1:p.His95=
ENST00000584950.5:c.285C>T	ENSP00000463582.1:p.His95=
NM_012452.2:c.423C>T , LRG_120t1:c.423C>T	NP_036584.1:p.His141=
NM_012452.3:c.423C>T MANE Select	NP_036584.1:p.His141=