Canonical Allele Identifier: CA397952665
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915922A>C (hg19) chr17:g.8012604A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012604A>C , CM000679.2:g.8012604A>C GRCh38
NC_000017.10:g.7915922A>C , CM000679.1:g.7915922A>C GRCh37
NC_000017.9:g.7856647A>C NCBI36
NG_009092.1:g.14935A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2111A>C MANE Select ENSP00000254854.4:p.Glu704Ala
ENST00000254854.4:c.2111A>C ENSP00000254854.4:p.Glu704Ala
NM_000180.3:c.2111A>C NP_000171.1:p.Glu704Ala
XM_011523816.1:c.2111A>C XP_011522118.1:p.Glu704Ala
NM_000180.4:c.2111A>C MANE Select NP_000171.1:p.Glu704Ala
Search 100 bp 5'
Search 100 bp 3'