Canonical Allele Identifier: CA624997622

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1346367061
• gnomAD v2: 17-16845017-A-G
• MyVariant Identifiers: chr17:g.16845017A>G (hg19) ; chr17:g.16941703A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941703A>G , CM000679.2:g.16941703A>G	GRCh38
NC_000017.10:g.16845017A>G , CM000679.1:g.16845017A>G	GRCh37
NC_000017.9:g.16785742A>G	NCBI36
NG_007281.1:g.35386T>C , LRG_120:g.35386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1192T>C MANE Select	ENSP00000261652.2:n.446-1192T>C
ENST00000261652.6:c.446-1192T>C	ENSP00000261652.2:n.446-1192T>C
ENST00000579315.5:c.445+7035T>C	ENSP00000464069.1:n.445+7035T>C
ENST00000581616.2:n.449-226T>C
ENST00000582931.5:n.349+7035T>C
ENST00000583789.1:c.308-1192T>C	ENSP00000462952.1:n.308-1192T>C
ENST00000584950.5:c.308-1192T>C	ENSP00000463582.1:n.308-1192T>C
NM_012452.2:c.446-1192T>C , LRG_120t1:c.446-1192T>C	NP_036584.1:n.446-1192T>C
NM_012452.3:c.446-1192T>C MANE Select	NP_036584.1:n.446-1192T>C