Canonical Allele Identifier: CA397943838
Gene: GUCY2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003528A>T , CM000679.2:g.8003528A>T GRCh38
NC_000017.10:g.7906846A>T , CM000679.1:g.7906846A>T GRCh37
NC_000017.9:g.7847571A>T NCBI36
NG_009092.1:g.5859A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.481A>T MANE Select ENSP00000254854.4:p.Thr161Ser
ENST00000254854.4:c.481A>T ENSP00000254854.4:p.Thr161Ser
NM_000180.3:c.481A>T NP_000171.1:p.Thr161Ser
XM_011523816.1:c.481A>T XP_011522118.1:p.Thr161Ser
NM_000180.4:c.481A>T MANE Select NP_000171.1:p.Thr161Ser