Canonical Allele Identifier: CA497953016
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7906965A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003647A>G , CM000679.2:g.8003647A>G GRCh38
NC_000017.10:g.7906965A>G , CM000679.1:g.7906965A>G GRCh37
NC_000017.9:g.7847690A>G NCBI36
NG_009092.1:g.5978A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000254854.5:c.600A>G MANE Select ENSP00000254854.4:p.Ser200=
ENST00000254854.4:c.600A>G ENSP00000254854.4:p.Ser200=
NM_000180.3:c.600A>G NP_000171.1:p.Ser200=
XM_011523816.1:c.600A>G XP_011522118.1:p.Ser200=
NM_000180.4:c.600A>G MANE Select NP_000171.1:p.Ser200=
Search 100 bp 5'
Search 100 bp 3'