Canonical Allele Identifier: CA625313736

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1216992003
• gnomAD v2: 17-16851970-C-G
• gnomAD v3: 17-16948656-C-G
• gnomAD v4: 17-16948656-C-G
• MyVariant Identifiers: chr17:g.16851970C>G (hg19) ; chr17:g.16948656C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948656C>G , CM000679.2:g.16948656C>G	GRCh38
NC_000017.10:g.16851970C>G , CM000679.1:g.16851970C>G	GRCh37
NC_000017.9:g.16792695C>G	NCBI36
NG_007281.1:g.28433G>C , LRG_120:g.28433G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+82G>C MANE Select	ENSP00000261652.2:n.445+82G>C
ENST00000261652.6:c.445+82G>C	ENSP00000261652.2:n.445+82G>C
ENST00000579315.5:c.445+82G>C	ENSP00000464069.1:n.445+82G>C
ENST00000581616.2:n.448+82G>C
ENST00000582931.5:n.349+82G>C
ENST00000583789.1:c.307+82G>C	ENSP00000462952.1:n.307+82G>C
ENST00000584950.5:c.307+82G>C	ENSP00000463582.1:n.307+82G>C
NM_012452.2:c.445+82G>C , LRG_120t1:c.445+82G>C	NP_036584.1:n.445+82G>C
NM_012452.3:c.445+82G>C MANE Select	NP_036584.1:n.445+82G>C