Canonical Allele Identifier: CA397952532
Gene: GUCY2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012569A>T , CM000679.2:g.8012569A>T GRCh38
NC_000017.10:g.7915887A>T , CM000679.1:g.7915887A>T GRCh37
NC_000017.9:g.7856612A>T NCBI36
NG_009092.1:g.14900A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2076A>T MANE Select ENSP00000254854.4:p.Glu692Asp
ENST00000254854.4:c.2076A>T ENSP00000254854.4:p.Glu692Asp
NM_000180.3:c.2076A>T NP_000171.1:p.Glu692Asp
XM_011523816.1:c.2076A>T XP_011522118.1:p.Glu692Asp
NM_000180.4:c.2076A>T MANE Select NP_000171.1:p.Glu692Asp