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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA8365518
Gene: GUCY2D
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2042450
ClinVar RCV Id:
RCV002895559
dbSNP Id:
rs546417010
ExAC:
17:7906974 G / A
gnomAD v2:
17-7906974-G-A
gnomAD v3:
17-8003656-G-A
gnomAD v4:
17-8003656-G-A
MyVariant Identifiers:
chr17:g.7906974G>A (hg19)
chr17:g.8003656G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.8003656G>A , CM000679.2:g.8003656G>A
GRCh38
NC_000017.10:g.7906974G>A , CM000679.1:g.7906974G>A
GRCh37
NC_000017.9:g.7847699G>A
NCBI36
NG_009092.1:g.5987G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000254854.5:c.609G>A
MANE Select
ENSP00000254854.4:p.Thr203=
ENST00000254854.4:c.609G>A
ENSP00000254854.4:p.Thr203=
NM_000180.3:c.609G>A
NP_000171.1:p.Thr203=
XM_011523816.1:c.609G>A
XP_011522118.1:p.Thr203=
NM_000180.4:c.609G>A
MANE Select
NP_000171.1:p.Thr203=
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