Canonical Allele Identifier: CA498420308

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852224G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948910G>T , CM000679.2:g.16948910G>T	GRCh38
NC_000017.10:g.16852224G>T , CM000679.1:g.16852224G>T	GRCh37
NC_000017.9:g.16792949G>T	NCBI36
NG_007281.1:g.28179C>A , LRG_120:g.28179C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.273C>A MANE Select	ENSP00000261652.2:p.Ser91=
ENST00000261652.6:c.273C>A	ENSP00000261652.2:p.Ser91=
ENST00000579315.5:c.273C>A	ENSP00000464069.1:p.Ser91=
ENST00000581616.2:n.276C>A
ENST00000582931.5:n.177C>A
ENST00000583789.1:c.135C>A	ENSP00000462952.1:p.Ser45=
ENST00000584950.5:c.135C>A	ENSP00000463582.1:p.Ser45=
NM_012452.2:c.273C>A , LRG_120t1:c.273C>A	NP_036584.1:p.Ser91=
NM_012452.3:c.273C>A MANE Select	NP_036584.1:p.Ser91=