Canonical Allele Identifier: CA2250305229

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948975T= , CM000679.2:g.16948975T=	GRCh38
NC_000017.10:g.16852289T= , CM000679.1:g.16852289T=	GRCh37
NC_000017.9:g.16793014T=	NCBI36
NG_007281.1:g.28114A= , LRG_120:g.28114A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.208A= MANE Select	ENSP00000261652.2:p.Ser70=
ENST00000261652.6:c.208A=	ENSP00000261652.2:p.Ser70=
ENST00000579315.5:c.208A=	ENSP00000464069.1:p.Ser70=
ENST00000581616.2:n.211A=
ENST00000582931.5:n.112A=
ENST00000583789.1:c.70A=	ENSP00000462952.1:p.Ser24=
ENST00000584950.5:c.70A=	ENSP00000463582.1:p.Ser24=
NM_012452.2:c.208A= , LRG_120t1:c.208A=	NP_036584.1:p.Ser70=
NM_012452.3:c.208A= MANE Select	NP_036584.1:p.Ser70=