Canonical Allele Identifier: CA398520203
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852271C>G (hg19) chr17:g.16948957C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948957C>G , CM000679.2:g.16948957C>G GRCh38
NC_000017.10:g.16852271C>G , CM000679.1:g.16852271C>G GRCh37
NC_000017.9:g.16792996C>G NCBI36
NG_007281.1:g.28132G>C , LRG_120:g.28132G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.226G>C MANE Select ENSP00000261652.2:p.Gly76Arg
ENST00000261652.6:c.226G>C ENSP00000261652.2:p.Gly76Arg
ENST00000579315.5:c.226G>C ENSP00000464069.1:p.Gly76Arg
ENST00000581616.2:n.229G>C
ENST00000582931.5:n.130G>C
ENST00000583789.1:c.88G>C ENSP00000462952.1:p.Gly30Arg
ENST00000584950.5:c.88G>C ENSP00000463582.1:p.Gly30Arg
NM_012452.2:c.226G>C , LRG_120t1:c.226G>C NP_036584.1:p.Gly76Arg
NM_012452.3:c.226G>C MANE Select NP_036584.1:p.Gly76Arg
Search 100 bp 5'
Search 100 bp 3'