Canonical Allele Identifier: CA8365999
Gene: GUCY2D HGNC NCBI

Linked Data

dbSNP Id: rs373788984
ExAC: 17:7915951 T / A
gnomAD v2: 17-7915951-T-A
gnomAD v4: 17-8012633-T-A
MyVariant Identifiers: chr17:g.7915951T>A (hg19) chr17:g.7915951_7915952delinsAC (hg19) chr17:g.8012633T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012633T>A , CM000679.2:g.8012633T>A GRCh38
NC_000017.10:g.7915951T>A , CM000679.1:g.7915951T>A GRCh37
NC_000017.9:g.7856676T>A NCBI36
NG_009092.1:g.14964T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2113+27T>A MANE Select ENSP00000254854.4:n.2113+27T>A
ENST00000254854.4:c.2113+27T>A ENSP00000254854.4:n.2113+27T>A
NM_000180.3:c.2113+27T>A NP_000171.1:n.2113+27T>A
XM_011523816.1:c.2113+27T>A XP_011522118.1:n.2113+27T>A
NM_000180.4:c.2113+27T>A MANE Select NP_000171.1:n.2113+27T>A
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