Canonical Allele Identifier: CA14418272
Gene: TNFRSF13B HGNC NCBI
COSMIC:
COSN6653549 (not active)
MyVariant.info:
GRCh38 chr17:g.16945436C>T
GRCh37 chr17:g.16848750C>T
gnomAD v2:
17:16848750 C / T
gnomAD v3:
17:16945436 C / T
gnomAD v4:
chr17-16945436-C-T
Joint Max Group AF 0.3833809 (EAS)
Genomes Max Group AF 0.3833809 (EAS)
dbSNP:
4561508
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16945436C>T , CM000679.2:g.16945436C>T GRCh38
NC_000017.10:g.16848750C>T , CM000679.1:g.16848750C>T GRCh37
NC_000017.9:g.16789475C>T NCBI36
NG_007281.1:g.31653G>A , LRG_120:g.31653G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.445+3302G>A MANE Select ENSP00000261652.2:n.445+3302G>A
ENST00000261652.6:c.445+3302G>A ENSP00000261652.2:n.445+3302G>A
ENST00000579315.5:c.445+3302G>A ENSP00000464069.1:n.445+3302G>A
ENST00000581616.2:n.448+3302G>A
ENST00000582931.5:n.349+3302G>A
ENST00000583789.1:c.307+3302G>A ENSP00000462952.1:n.307+3302G>A
ENST00000584950.5:c.307+3302G>A ENSP00000463582.1:n.307+3302G>A
NM_012452.2:c.445+3302G>A , LRG_120t1:c.445+3302G>A NP_036584.1:n.445+3302G>A
NM_012452.3:c.445+3302G>A MANE Select NP_036584.1:n.445+3302G>A
Search 100 bp 5'
Search 100 bp 3'