Canonical Allele Identifier: CA566286819
Gene: TDP2 HGNC NCBI

Linked Data

dbSNP Id: rs1163616826
gnomAD v2: 6-24658723-A-C
MyVariant Identifiers: chr6:g.24658723A>C (hg19) chr6:g.24658495A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658495A>C , CM000668.2:g.24658495A>C GRCh38
NC_000006.11:g.24658723A>C , CM000668.1:g.24658723A>C GRCh37
NC_000006.10:g.24766702A>C NCBI36
NG_052787.1:g.13393T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+66T>G MANE Select ENSP00000367440.4:n.425+66T>G
ENST00000341060.3:c.251+66T>G ENSP00000345345.3:n.251+66T>G
ENST00000378198.8:c.425+66T>G ENSP00000367440.4:n.425+66T>G
ENST00000478285.1:n.612+66T>G
ENST00000478507.1:n.320-5342T>G
NM_016614.2:c.425+66T>G NP_057698.2:n.425+66T>G
XR_926244.1:n.552+66T>G
NM_016614.3:c.425+66T>G MANE Select NP_057698.2:n.425+66T>G
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