Canonical Allele Identifier: CA497953038
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7906974G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003656G>C , CM000679.2:g.8003656G>C GRCh38
NC_000017.10:g.7906974G>C , CM000679.1:g.7906974G>C GRCh37
NC_000017.9:g.7847699G>C NCBI36
NG_009092.1:g.5987G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000254854.5:c.609G>C MANE Select ENSP00000254854.4:p.Thr203=
ENST00000254854.4:c.609G>C ENSP00000254854.4:p.Thr203=
NM_000180.3:c.609G>C NP_000171.1:p.Thr203=
XM_011523816.1:c.609G>C XP_011522118.1:p.Thr203=
NM_000180.4:c.609G>C MANE Select NP_000171.1:p.Thr203=
Search 100 bp 5'
Search 100 bp 3'