Canonical Allele Identifier: CA226058
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 98551
ClinVar RCV Id: RCV000084844
dbSNP Id: rs61749759
MyVariant Identifiers: chr17:g.7915767G>A (hg19) chr17:g.8012449G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012449G>A , CM000679.2:g.8012449G>A GRCh38
NC_000017.10:g.7915767G>A , CM000679.1:g.7915767G>A GRCh37
NC_000017.9:g.7856492G>A NCBI36
NG_009092.1:g.14780G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1957-1G>A MANE Select ENSP00000254854.4:n.1957-1G>A
ENST00000254854.4:c.1957-1G>A ENSP00000254854.4:n.1957-1G>A
NM_000180.3:c.1957-1G>A NP_000171.1:n.1957-1G>A
XM_011523816.1:c.1957-1G>A XP_011522118.1:n.1957-1G>A
NM_000180.4:c.1957-1G>A MANE Select NP_000171.1:n.1957-1G>A
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