Canonical Allele Identifier: CA733685144
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1488141655
gnomAD v3: 1-241847995-C-A
gnomAD v4: 1-241847995-C-A
MyVariant Identifiers: chr1:g.242011297C>A (hg19) chr1:g.241847995C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241847995C>A , CM000663.2:g.241847995C>A GRCh38
NC_000001.10:g.242011297C>A , CM000663.1:g.242011297C>A GRCh37
NC_000001.9:g.240077920C>A NCBI36
NG_029100.1:g.4805C>A
NG_029100.2:g.4805C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000519225.5:c.-520C>A ENSP00000429720.1:n.-520C>A
XM_011544322.1:c.-520C>A XP_011542624.1:n.-520C>A
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