Canonical Allele Identifier: CA40385046
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs965532538
gnomAD v3: 1-241889949-A-G
gnomAD v4: 1-241889949-A-G
MyVariant Identifiers: chr1:g.242053251A>G (hg19) chr1:g.241889949A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241889949A>G , CM000663.2:g.241889949A>G GRCh38
NC_000001.10:g.242053251A>G , CM000663.1:g.242053251A>G GRCh37
NC_000001.9:g.240119874A>G NCBI36
NG_029100.1:g.46759A>G
NG_029100.2:g.46759A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518741.1:n.152-2575A>G
XR_949162.1:n.2990+4442A>G
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