Canonical Allele Identifier: CA398520266
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852299T>A (hg19) chr17:g.16948985T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948985T>A , CM000679.2:g.16948985T>A GRCh38
NC_000017.10:g.16852299T>A , CM000679.1:g.16852299T>A GRCh37
NC_000017.9:g.16793024T>A NCBI36
NG_007281.1:g.28104A>T , LRG_120:g.28104A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.200-2A>T MANE Select ENSP00000261652.2:n.200-2A>T
ENST00000261652.6:c.200-2A>T ENSP00000261652.2:n.200-2A>T
ENST00000579315.5:c.200-2A>T ENSP00000464069.1:n.200-2A>T
ENST00000581616.2:n.203-2A>T
ENST00000582931.5:n.104-2A>T
ENST00000583789.1:c.62-2A>T ENSP00000462952.1:n.62-2A>T
ENST00000584950.5:c.62-2A>T ENSP00000463582.1:n.62-2A>T
NM_012452.2:c.200-2A>T , LRG_120t1:c.200-2A>T NP_036584.1:n.200-2A>T
NM_012452.3:c.200-2A>T MANE Select NP_036584.1:n.200-2A>T
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