Canonical Allele Identifier: CA226062
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 98554
ClinVar RCV Id: RCV000084847 RCV001047937 RCV001250870
dbSNP Id: rs61750161
gnomAD v2: 17-7915789-C-T
gnomAD v3: 17-8012471-C-T
gnomAD v4: 17-8012471-C-T
MyVariant Identifiers: chr17:g.7915789C>T (hg19) chr17:g.8012471C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012471C>T , CM000679.2:g.8012471C>T GRCh38
NC_000017.10:g.7915789C>T , CM000679.1:g.7915789C>T GRCh37
NC_000017.9:g.7856514C>T NCBI36
NG_009092.1:g.14802C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1978C>T MANE Select ENSP00000254854.4:p.Arg660Ter
ENST00000254854.4:c.1978C>T ENSP00000254854.4:p.Arg660Ter
NM_000180.3:c.1978C>T NP_000171.1:p.Arg660Ter
XM_011523816.1:c.1978C>T XP_011522118.1:p.Arg660Ter
NM_000180.4:c.1978C>T MANE Select NP_000171.1:p.Arg660Ter
Search 100 bp 5'
Search 100 bp 3'