Canonical Allele Identifier: CA497753820
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7919071G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8015753G>T , CM000679.2:g.8015753G>T GRCh38
NC_000017.10:g.7919071G>T , CM000679.1:g.7919071G>T GRCh37
NC_000017.9:g.7859796G>T NCBI36
NG_009092.1:g.18084G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.2955G>T MANE Select ENSP00000254854.4:p.Val985=
ENST00000254854.4:c.2955G>T ENSP00000254854.4:p.Val985=
NM_000180.3:c.2955G>T NP_000171.1:p.Val985=
XM_011523816.1:c.2955G>T XP_011522118.1:p.Val985=
NM_000180.4:c.2955G>T MANE Select NP_000171.1:p.Val985=