Canonical Allele Identifier: CA213295958
Gene: GUCY2GP HGNC NCBI

Linked Data

dbSNP Id: rs537493705
gnomAD v2: 10-114079031-T-G
gnomAD v3: 10-112319273-T-G
gnomAD v4: 10-112319273-T-G
MyVariant Identifiers: chr10:g.114079031T>G (hg19) chr10:g.112319273T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112319273T>G , CM000672.2:g.112319273T>G GRCh38
NC_000010.10:g.114079031T>G , CM000672.1:g.114079031T>G GRCh37
NC_000010.9:g.114069021T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000479705.5:n.2245-1217A>C
ENST00000490269.1:n.461-1217A>C
NR_028134.1:n.1994-1217A>C
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