Canonical Allele Identifier: CA2250304857

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948878T= , CM000679.2:g.16948878T=	GRCh38
NC_000017.10:g.16852192T= , CM000679.1:g.16852192T=	GRCh37
NC_000017.9:g.16792917T=	NCBI36
NG_007281.1:g.28211A= , LRG_120:g.28211A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.305A= MANE Select	ENSP00000261652.2:p.Tyr102=
ENST00000261652.6:c.305A=	ENSP00000261652.2:p.Tyr102=
ENST00000579315.5:c.305A=	ENSP00000464069.1:p.Tyr102=
ENST00000581616.2:n.308A=
ENST00000582931.5:n.209A=
ENST00000583789.1:c.167A=	ENSP00000462952.1:p.Tyr56=
ENST00000584950.5:c.167A=	ENSP00000463582.1:p.Tyr56=
NM_012452.2:c.305A= , LRG_120t1:c.305A=	NP_036584.1:p.Tyr102=
NM_012452.3:c.305A= MANE Select	NP_036584.1:p.Tyr102=