Canonical Allele Identifier: CA498420327
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1227980908
gnomAD v2: 17-16852254-A-G
gnomAD v4: 17-16948940-A-G
COSMIC: COSM4932398 COSM4932399
MyVariant Identifiers: chr17:g.16852254A>G (hg19) chr17:g.16948940A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948940A>G , CM000679.2:g.16948940A>G GRCh38
NC_000017.10:g.16852254A>G , CM000679.1:g.16852254A>G GRCh37
NC_000017.9:g.16792979A>G NCBI36
NG_007281.1:g.28149T>C , LRG_120:g.28149T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.243T>C MANE Select ENSP00000261652.2:p.His81=
ENST00000261652.6:c.243T>C ENSP00000261652.2:p.His81=
ENST00000579315.5:c.243T>C ENSP00000464069.1:p.His81=
ENST00000581616.2:n.246T>C
ENST00000582931.5:n.147T>C
ENST00000583789.1:c.105T>C ENSP00000462952.1:p.His35=
ENST00000584950.5:c.105T>C ENSP00000463582.1:p.His35=
NM_012452.2:c.243T>C , LRG_120t1:c.243T>C NP_036584.1:p.His81=
NM_012452.3:c.243T>C MANE Select NP_036584.1:p.His81=
Search 100 bp 5'
Search 100 bp 3'