Canonical Allele Identifier: CA8414071
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs562284274
ExAC: 17:16852292 G / A
gnomAD v2: 17-16852292-G-A
gnomAD v3: 17-16948978-G-A
gnomAD v4: 17-16948978-G-A
MyVariant Identifiers: chr17:g.16852292G>A (hg19) chr17:g.16948978G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948978G>A , CM000679.2:g.16948978G>A GRCh38
NC_000017.10:g.16852292G>A , CM000679.1:g.16852292G>A GRCh37
NC_000017.9:g.16793017G>A NCBI36
NG_007281.1:g.28111C>T , LRG_120:g.28111C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.205C>T MANE Select ENSP00000261652.2:p.Leu69Phe
ENST00000261652.6:c.205C>T ENSP00000261652.2:p.Leu69Phe
ENST00000579315.5:c.205C>T ENSP00000464069.1:p.Leu69Phe
ENST00000581616.2:n.208C>T
ENST00000582931.5:n.109C>T
ENST00000583789.1:c.67C>T ENSP00000462952.1:p.Leu23Phe
ENST00000584950.5:c.67C>T ENSP00000463582.1:p.Leu23Phe
NM_012452.2:c.205C>T , LRG_120t1:c.205C>T NP_036584.1:p.Leu69Phe
NM_012452.3:c.205C>T MANE Select NP_036584.1:p.Leu69Phe
Search 100 bp 5'
Search 100 bp 3'