Canonical Allele Identifier: CA2677539721
Gene: TDP2 HGNC NCBI

Linked Data

gnomAD v4: 6-24658474-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658474G>T , CM000668.2:g.24658474G>T GRCh38
NC_000006.11:g.24658702G>T , CM000668.1:g.24658702G>T GRCh37
NC_000006.10:g.24766681G>T NCBI36
NG_052787.1:g.13414C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+87C>A MANE Select ENSP00000367440.4:n.425+87C>A
ENST00000341060.3:c.251+87C>A ENSP00000345345.3:n.251+87C>A
ENST00000378198.8:c.425+87C>A ENSP00000367440.4:n.425+87C>A
ENST00000478285.1:n.612+87C>A
ENST00000478507.1:n.320-5321C>A
NM_016614.2:c.425+87C>A NP_057698.2:n.425+87C>A
XR_926244.1:n.552+87C>A
NM_016614.3:c.425+87C>A MANE Select NP_057698.2:n.425+87C>A
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