Canonical Allele Identifier: CA8413995

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs781625740
• ExAC: 17:16852006 T / A
• gnomAD v2: 17-16852006-T-A
• gnomAD v4: 17-16948692-T-A
• MyVariant Identifiers: chr17:g.16852006T>A (hg19) ; chr17:g.16948692T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948692T>A , CM000679.2:g.16948692T>A	GRCh38
NC_000017.10:g.16852006T>A , CM000679.1:g.16852006T>A	GRCh37
NC_000017.9:g.16792731T>A	NCBI36
NG_007281.1:g.28397A>T , LRG_120:g.28397A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.445+46A>T MANE Select	ENSP00000261652.2:n.445+46A>T
ENST00000261652.6:c.445+46A>T	ENSP00000261652.2:n.445+46A>T
ENST00000579315.5:c.445+46A>T	ENSP00000464069.1:n.445+46A>T
ENST00000581616.2:n.448+46A>T
ENST00000582931.5:n.349+46A>T
ENST00000583789.1:c.307+46A>T	ENSP00000462952.1:n.307+46A>T
ENST00000584950.5:c.307+46A>T	ENSP00000463582.1:n.307+46A>T
NM_012452.2:c.445+46A>T , LRG_120t1:c.445+46A>T	NP_036584.1:n.445+46A>T
NM_012452.3:c.445+46A>T MANE Select	NP_036584.1:n.445+46A>T