Canonical Allele Identifier: CA397955185
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7919090A>G (hg19) chr17:g.8015772A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8015772A>G , CM000679.2:g.8015772A>G GRCh38
NC_000017.10:g.7919090A>G , CM000679.1:g.7919090A>G GRCh37
NC_000017.9:g.7859815A>G NCBI36
NG_009092.1:g.18103A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2974A>G MANE Select ENSP00000254854.4:p.Thr992Ala
ENST00000254854.4:c.2974A>G ENSP00000254854.4:p.Thr992Ala
NM_000180.3:c.2974A>G NP_000171.1:p.Thr992Ala
XM_011523816.1:c.2974A>G XP_011522118.1:p.Thr992Ala
NM_000180.4:c.2974A>G MANE Select NP_000171.1:p.Thr992Ala
Search 100 bp 5'
Search 100 bp 3'