Canonical Allele Identifier: CA497953116
Gene: GUCY2D HGNC NCBI

Linked Data

dbSNP Id: rs1254415576
MyVariant Identifiers: chr17:g.7915770A>C (hg19) chr17:g.8012452A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012452A>C , CM000679.2:g.8012452A>C GRCh38
NC_000017.10:g.7915770A>C , CM000679.1:g.7915770A>C GRCh37
NC_000017.9:g.7856495A>C NCBI36
NG_009092.1:g.14783A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1959A>C MANE Select ENSP00000254854.4:p.Gly653=
ENST00000254854.4:c.1959A>C ENSP00000254854.4:p.Gly653=
NM_000180.3:c.1959A>C NP_000171.1:p.Gly653=
XM_011523816.1:c.1959A>C XP_011522118.1:p.Gly653=
NM_000180.4:c.1959A>C MANE Select NP_000171.1:p.Gly653=
Search 100 bp 5'
Search 100 bp 3'