Canonical Allele Identifier: CA40385048
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs967629189
gnomAD v3: 1-241889960-T-G
gnomAD v4: 1-241889960-T-G
MyVariant Identifiers: chr1:g.242053262T>G (hg19) chr1:g.241889960T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241889960T>G , CM000663.2:g.241889960T>G GRCh38
NC_000001.10:g.242053262T>G , CM000663.1:g.242053262T>G GRCh37
NC_000001.9:g.240119885T>G NCBI36
NG_029100.1:g.46770T>G
NG_029100.2:g.46770T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518741.1:n.152-2564T>G
XR_949162.1:n.2990+4453T>G
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