Canonical Allele Identifier: CA288283977

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs8079680
• gnomAD v2: 17-16845230-A-G
• gnomAD v3: 17-16941916-A-G
• gnomAD v4: 17-16941916-A-G
• MyVariant Identifiers: chr17:g.16845230A>G (hg19) ; chr17:g.16941916A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941916A>G , CM000679.2:g.16941916A>G	GRCh38
NC_000017.10:g.16845230A>G , CM000679.1:g.16845230A>G	GRCh37
NC_000017.9:g.16785955A>G	NCBI36
NG_007281.1:g.35173T>C , LRG_120:g.35173T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.446-1405T>C MANE Select	ENSP00000261652.2:n.446-1405T>C
ENST00000261652.6:c.446-1405T>C	ENSP00000261652.2:n.446-1405T>C
ENST00000579315.5:c.445+6822T>C	ENSP00000464069.1:n.445+6822T>C
ENST00000581616.2:n.449-439T>C
ENST00000582931.5:n.349+6822T>C
ENST00000583789.1:c.308-1405T>C	ENSP00000462952.1:n.308-1405T>C
ENST00000584950.5:c.308-1405T>C	ENSP00000463582.1:n.308-1405T>C
NM_012452.2:c.446-1405T>C , LRG_120t1:c.446-1405T>C	NP_036584.1:n.446-1405T>C
NM_012452.3:c.446-1405T>C MANE Select	NP_036584.1:n.446-1405T>C