Canonical Allele Identifier: CA497952832
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 2951060
ClinVar RCV Id: RCV003802322
gnomAD v4: 17-8003515-G-A
MyVariant Identifiers: chr17:g.7906833G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003515G>A , CM000679.2:g.8003515G>A GRCh38
NC_000017.10:g.7906833G>A , CM000679.1:g.7906833G>A GRCh37
NC_000017.9:g.7847558G>A NCBI36
NG_009092.1:g.5846G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.468G>A MANE Select ENSP00000254854.4:p.Gln156=
ENST00000254854.4:c.468G>A ENSP00000254854.4:p.Gln156=
NM_000180.3:c.468G>A NP_000171.1:p.Gln156=
XM_011523816.1:c.468G>A XP_011522118.1:p.Gln156=
NM_000180.4:c.468G>A MANE Select NP_000171.1:p.Gln156=
Search 100 bp 5'
Search 100 bp 3'