Canonical Allele Identifier: CA226059
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 98552
ClinVar RCV Id: RCV000084845 RCV001250862
dbSNP Id: rs61749759
MyVariant Identifiers: chr17:g.7915767G>T (hg19) chr17:g.8012449G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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