Canonical Allele Identifier: CA8414062
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1536731
ClinVar RCV Id: RCV002166781
dbSNP Id: rs371317735
ExAC: 17:16852266 C / T
gnomAD v2: 17-16852266-C-T
gnomAD v3: 17-16948952-C-T
gnomAD v4: 17-16948952-C-T
MyVariant Identifiers: chr17:g.16852266C>T (hg19) chr17:g.16948952C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948952C>T , CM000679.2:g.16948952C>T GRCh38
NC_000017.10:g.16852266C>T , CM000679.1:g.16852266C>T GRCh37
NC_000017.9:g.16792991C>T NCBI36
NG_007281.1:g.28137G>A , LRG_120:g.28137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.231G>A MANE Select ENSP00000261652.2:p.Lys77=
ENST00000261652.6:c.231G>A ENSP00000261652.2:p.Lys77=
ENST00000579315.5:c.231G>A ENSP00000464069.1:p.Lys77=
ENST00000581616.2:n.234G>A
ENST00000582931.5:n.135G>A
ENST00000583789.1:c.93G>A ENSP00000462952.1:p.Lys31=
ENST00000584950.5:c.93G>A ENSP00000463582.1:p.Lys31=
NM_012452.2:c.231G>A , LRG_120t1:c.231G>A NP_036584.1:p.Lys77=
NM_012452.3:c.231G>A MANE Select NP_036584.1:p.Lys77=
Search 100 bp 5'
Search 100 bp 3'