Canonical Allele Identifier: CA498420306

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948910-G-A
• MyVariant Identifiers: chr17:g.16852224G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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