Canonical Allele Identifier: CA659950269
Gene: GUCY2GP HGNC NCBI

Linked Data

dbSNP Id: rs1392305896
gnomAD v3: 10-112318966-T-C
gnomAD v4: 10-112318966-T-C
MyVariant Identifiers: chr10:g.114078724T>C (hg19) chr10:g.112318966T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112318966T>C , CM000672.2:g.112318966T>C GRCh38
NC_000010.10:g.114078724T>C , CM000672.1:g.114078724T>C GRCh37
NC_000010.9:g.114068714T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000479705.5:n.2245-910A>G
ENST00000490269.1:n.461-910A>G
NR_028134.1:n.1994-910A>G
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