Canonical Allele Identifier: CA136164864
Gene: TDP2 HGNC NCBI

Linked Data

dbSNP Id: rs895455135
gnomAD v2: 6-24658710-T-C
gnomAD v3: 6-24658482-T-C
gnomAD v4: 6-24658482-T-C
MyVariant Identifiers: chr6:g.24658710T>C (hg19) chr6:g.24658482T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658482T>C , CM000668.2:g.24658482T>C GRCh38
NC_000006.11:g.24658710T>C , CM000668.1:g.24658710T>C GRCh37
NC_000006.10:g.24766689T>C NCBI36
NG_052787.1:g.13406A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+79A>G MANE Select ENSP00000367440.4:n.425+79A>G
ENST00000341060.3:c.251+79A>G ENSP00000345345.3:n.251+79A>G
ENST00000378198.8:c.425+79A>G ENSP00000367440.4:n.425+79A>G
ENST00000478285.1:n.612+79A>G
ENST00000478507.1:n.320-5329A>G
NM_016614.2:c.425+79A>G NP_057698.2:n.425+79A>G
XR_926244.1:n.552+79A>G
NM_016614.3:c.425+79A>G MANE Select NP_057698.2:n.425+79A>G
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