Canonical Allele Identifier: CA397952055
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915777T>G (hg19) chr17:g.8012459T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012459T>G , CM000679.2:g.8012459T>G GRCh38
NC_000017.10:g.7915777T>G , CM000679.1:g.7915777T>G GRCh37
NC_000017.9:g.7856502T>G NCBI36
NG_009092.1:g.14790T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1966T>G MANE Select ENSP00000254854.4:p.Tyr656Asp
ENST00000254854.4:c.1966T>G ENSP00000254854.4:p.Tyr656Asp
NM_000180.3:c.1966T>G NP_000171.1:p.Tyr656Asp
XM_011523816.1:c.1966T>G XP_011522118.1:p.Tyr656Asp
NM_000180.4:c.1966T>G MANE Select NP_000171.1:p.Tyr656Asp
Search 100 bp 5'
Search 100 bp 3'