Canonical Allele Identifier: CA497953009
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7906962C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003644C>A , CM000679.2:g.8003644C>A GRCh38
NC_000017.10:g.7906962C>A , CM000679.1:g.7906962C>A GRCh37
NC_000017.9:g.7847687C>A NCBI36
NG_009092.1:g.5975C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000254854.5:c.597C>A MANE Select ENSP00000254854.4:p.Arg199=
ENST00000254854.4:c.597C>A ENSP00000254854.4:p.Arg199=
NM_000180.3:c.597C>A NP_000171.1:p.Arg199=
XM_011523816.1:c.597C>A XP_011522118.1:p.Arg199=
NM_000180.4:c.597C>A MANE Select NP_000171.1:p.Arg199=
Search 100 bp 5'
Search 100 bp 3'