Canonical Allele Identifier: CA497953475
Gene: GUCY2D HGNC NCBI

Linked Data

ClinVar Variation Id: 2950496
ClinVar RCV Id: RCV003809806
MyVariant Identifiers: chr17:g.7915914C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012596C>T , CM000679.2:g.8012596C>T GRCh38
NC_000017.10:g.7915914C>T , CM000679.1:g.7915914C>T GRCh37
NC_000017.9:g.7856639C>T NCBI36
NG_009092.1:g.14927C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2103C>T MANE Select ENSP00000254854.4:p.Pro701=
ENST00000254854.4:c.2103C>T ENSP00000254854.4:p.Pro701=
NM_000180.3:c.2103C>T NP_000171.1:p.Pro701=
XM_011523816.1:c.2103C>T XP_011522118.1:p.Pro701=
NM_000180.4:c.2103C>T MANE Select NP_000171.1:p.Pro701=
Search 100 bp 5'
Search 100 bp 3'