Canonical Allele Identifier: CA8414046
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2994681
ClinVar RCV Id: RCV003858304 RCV003909192
dbSNP Id: rs752990010
ExAC: 17:16852194 T / A
gnomAD v2: 17-16852194-T-A
gnomAD v4: 17-16948880-T-A
COSMIC: COSM6221721 COSM6221722
MyVariant Identifiers: chr17:g.16852194T>A (hg19) chr17:g.16948880T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948880T>A , CM000679.2:g.16948880T>A GRCh38
NC_000017.10:g.16852194T>A , CM000679.1:g.16852194T>A GRCh37
NC_000017.9:g.16792919T>A NCBI36
NG_007281.1:g.28209A>T , LRG_120:g.28209A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.303A>T MANE Select ENSP00000261652.2:p.Ala101=
ENST00000261652.6:c.303A>T ENSP00000261652.2:p.Ala101=
ENST00000579315.5:c.303A>T ENSP00000464069.1:p.Ala101=
ENST00000581616.2:n.306A>T
ENST00000582931.5:n.207A>T
ENST00000583789.1:c.165A>T ENSP00000462952.1:p.Ala55=
ENST00000584950.5:c.165A>T ENSP00000463582.1:p.Ala55=
NM_012452.2:c.303A>T , LRG_120t1:c.303A>T NP_036584.1:p.Ala101=
NM_012452.3:c.303A>T MANE Select NP_036584.1:p.Ala101=
Search 100 bp 5'
Search 100 bp 3'