Canonical Allele Identifier: CA733685170
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1487624909
gnomAD v3: 1-241848054-A-C
gnomAD v4: 1-241848054-A-C
MyVariant Identifiers: chr1:g.242011356A>C (hg19) chr1:g.241848054A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241848054A>C , CM000663.2:g.241848054A>C GRCh38
NC_000001.10:g.242011356A>C , CM000663.1:g.242011356A>C GRCh37
NC_000001.9:g.240077979A>C NCBI36
NG_029100.1:g.4864A>C
NG_029100.2:g.4864A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000519225.5:c.-461A>C ENSP00000429720.1:n.-461A>C
XM_011544322.1:c.-461A>C XP_011542624.1:n.-461A>C
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