Canonical Allele Identifier: CA823329090
Gene: TDP2 HGNC NCBI

Linked Data

dbSNP Id: rs1228889556
gnomAD v3: 6-24658467-G-C
gnomAD v4: 6-24658467-G-C
MyVariant Identifiers: chr6:g.24658695G>C (hg19) chr6:g.24658467G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658467G>C , CM000668.2:g.24658467G>C GRCh38
NC_000006.11:g.24658695G>C , CM000668.1:g.24658695G>C GRCh37
NC_000006.10:g.24766674G>C NCBI36
NG_052787.1:g.13421C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+94C>G MANE Select ENSP00000367440.4:n.425+94C>G
ENST00000341060.3:c.251+94C>G ENSP00000345345.3:n.251+94C>G
ENST00000378198.8:c.425+94C>G ENSP00000367440.4:n.425+94C>G
ENST00000478285.1:n.612+94C>G
ENST00000478507.1:n.320-5314C>G
NM_016614.2:c.425+94C>G NP_057698.2:n.425+94C>G
XR_926244.1:n.552+94C>G
NM_016614.3:c.425+94C>G MANE Select NP_057698.2:n.425+94C>G
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