Canonical Allele Identifier: CA497953252
Gene: GUCY2D HGNC NCBI

Linked Data

dbSNP Id: rs1975866076
MyVariant Identifiers: chr17:g.7915578C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012260C>T , CM000679.2:g.8012260C>T GRCh38
NC_000017.10:g.7915578C>T , CM000679.1:g.7915578C>T GRCh37
NC_000017.9:g.7856303C>T NCBI36
NG_009092.1:g.14591C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1866C>T MANE Select ENSP00000254854.4:p.Cys622=
ENST00000254854.4:c.1866C>T ENSP00000254854.4:p.Cys622=
NM_000180.3:c.1866C>T NP_000171.1:p.Cys622=
XM_011523816.1:c.1866C>T XP_011522118.1:p.Cys622=
NM_000180.4:c.1866C>T MANE Select NP_000171.1:p.Cys622=