Canonical Allele Identifier: CA497753808
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1552847
ClinVar RCV Id: RCV002187251
dbSNP Id: rs1290360925
gnomAD v2: 17-7919062-T-C
MyVariant Identifiers: chr17:g.7919062T>C (hg19) chr17:g.8015744T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8015744T>C , CM000679.2:g.8015744T>C GRCh38
NC_000017.10:g.7919062T>C , CM000679.1:g.7919062T>C GRCh37
NC_000017.9:g.7859787T>C NCBI36
NG_009092.1:g.18075T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2946T>C MANE Select ENSP00000254854.4:p.Gly982=
ENST00000254854.4:c.2946T>C ENSP00000254854.4:p.Gly982=
NM_000180.3:c.2946T>C NP_000171.1:p.Gly982=
XM_011523816.1:c.2946T>C XP_011522118.1:p.Gly982=
NM_000180.4:c.2946T>C MANE Select NP_000171.1:p.Gly982=
Search 100 bp 5'
Search 100 bp 3'