Canonical Allele Identifier: CA398520029

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852190A>T (hg19) ; chr17:g.16948876A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948876A>T , CM000679.2:g.16948876A>T	GRCh38
NC_000017.10:g.16852190A>T , CM000679.1:g.16852190A>T	GRCh37
NC_000017.9:g.16792915A>T	NCBI36
NG_007281.1:g.28213T>A , LRG_120:g.28213T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.307T>A MANE Select	ENSP00000261652.2:p.Phe103Ile
ENST00000261652.6:c.307T>A	ENSP00000261652.2:p.Phe103Ile
ENST00000579315.5:c.307T>A	ENSP00000464069.1:p.Phe103Ile
ENST00000581616.2:n.310T>A
ENST00000582931.5:n.211T>A
ENST00000583789.1:c.169T>A	ENSP00000462952.1:p.Phe57Ile
ENST00000584950.5:c.169T>A	ENSP00000463582.1:p.Phe57Ile
NM_012452.2:c.307T>A , LRG_120t1:c.307T>A	NP_036584.1:p.Phe103Ile
NM_012452.3:c.307T>A MANE Select	NP_036584.1:p.Phe103Ile