Canonical Allele Identifier: CA497953472
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915914C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012596C>A , CM000679.2:g.8012596C>A GRCh38
NC_000017.10:g.7915914C>A , CM000679.1:g.7915914C>A GRCh37
NC_000017.9:g.7856639C>A NCBI36
NG_009092.1:g.14927C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2103C>A MANE Select ENSP00000254854.4:p.Pro701=
ENST00000254854.4:c.2103C>A ENSP00000254854.4:p.Pro701=
NM_000180.3:c.2103C>A NP_000171.1:p.Pro701=
XM_011523816.1:c.2103C>A XP_011522118.1:p.Pro701=
NM_000180.4:c.2103C>A MANE Select NP_000171.1:p.Pro701=