Canonical Allele Identifier: CA726572906
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1170358705
MyVariant Identifiers: chr17:g.16845065A>G (hg19) chr17:g.16941751A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941751A>G , CM000679.2:g.16941751A>G GRCh38
NC_000017.10:g.16845065A>G , CM000679.1:g.16845065A>G GRCh37
NC_000017.9:g.16785790A>G NCBI36
NG_007281.1:g.35338T>C , LRG_120:g.35338T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1240T>C MANE Select ENSP00000261652.2:n.446-1240T>C
ENST00000261652.6:c.446-1240T>C ENSP00000261652.2:n.446-1240T>C
ENST00000579315.5:c.445+6987T>C ENSP00000464069.1:n.445+6987T>C
ENST00000581616.2:n.449-274T>C
ENST00000582931.5:n.349+6987T>C
ENST00000583789.1:c.308-1240T>C ENSP00000462952.1:n.308-1240T>C
ENST00000584950.5:c.308-1240T>C ENSP00000463582.1:n.308-1240T>C
NM_012452.2:c.446-1240T>C , LRG_120t1:c.446-1240T>C NP_036584.1:n.446-1240T>C
NM_012452.3:c.446-1240T>C MANE Select NP_036584.1:n.446-1240T>C
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