Canonical Allele Identifier: CA497953021
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7906966C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003648C>T , CM000679.2:g.8003648C>T GRCh38
NC_000017.10:g.7906966C>T , CM000679.1:g.7906966C>T GRCh37
NC_000017.9:g.7847691C>T NCBI36
NG_009092.1:g.5979C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000254854.5:c.601C>T MANE Select ENSP00000254854.4:p.Leu201=
ENST00000254854.4:c.601C>T ENSP00000254854.4:p.Leu201=
NM_000180.3:c.601C>T NP_000171.1:p.Leu201=
XM_011523816.1:c.601C>T XP_011522118.1:p.Leu201=
NM_000180.4:c.601C>T MANE Select NP_000171.1:p.Leu201=
Search 100 bp 5'
Search 100 bp 3'