Canonical Allele Identifier: CA595736051
Gene: GUCY2GP HGNC NCBI

Linked Data

dbSNP Id: rs1344570226
gnomAD v2: 10-114079039-A-C
gnomAD v3: 10-112319281-A-C
gnomAD v4: 10-112319281-A-C
MyVariant Identifiers: chr10:g.114079039A>C (hg19) chr10:g.112319281A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112319281A>C , CM000672.2:g.112319281A>C GRCh38
NC_000010.10:g.114079039A>C , CM000672.1:g.114079039A>C GRCh37
NC_000010.9:g.114069029A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000479705.5:n.2245-1225T>G
ENST00000490269.1:n.461-1225T>G
NR_028134.1:n.1994-1225T>G
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