Canonical Allele Identifier: CA397952602
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915906G>A (hg19) chr17:g.8012588G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012588G>A , CM000679.2:g.8012588G>A GRCh38
NC_000017.10:g.7915906G>A , CM000679.1:g.7915906G>A GRCh37
NC_000017.9:g.7856631G>A NCBI36
NG_009092.1:g.14919G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2095G>A MANE Select ENSP00000254854.4:p.Glu699Lys
ENST00000254854.4:c.2095G>A ENSP00000254854.4:p.Glu699Lys
NM_000180.3:c.2095G>A NP_000171.1:p.Glu699Lys
XM_011523816.1:c.2095G>A XP_011522118.1:p.Glu699Lys
NM_000180.4:c.2095G>A MANE Select NP_000171.1:p.Glu699Lys
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