Canonical Allele Identifier: CA498420113

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852065T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948751T>A , CM000679.2:g.16948751T>A	GRCh38
NC_000017.10:g.16852065T>A , CM000679.1:g.16852065T>A	GRCh37
NC_000017.9:g.16792790T>A	NCBI36
NG_007281.1:g.28338A>T , LRG_120:g.28338A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.432A>T MANE Select	ENSP00000261652.2:p.Ser144=
ENST00000261652.6:c.432A>T	ENSP00000261652.2:p.Ser144=
ENST00000579315.5:c.432A>T	ENSP00000464069.1:p.Ser144=
ENST00000581616.2:n.435A>T
ENST00000582931.5:n.336A>T
ENST00000583789.1:c.294A>T	ENSP00000462952.1:p.Ser98=
ENST00000584950.5:c.294A>T	ENSP00000463582.1:p.Ser98=
NM_012452.2:c.432A>T , LRG_120t1:c.432A>T	NP_036584.1:p.Ser144=
NM_012452.3:c.432A>T MANE Select	NP_036584.1:p.Ser144=