Canonical Allele Identifier: CA397943976
Gene: GUCY2D HGNC NCBI

Linked Data

gnomAD v4: 17-8003559-C-T
MyVariant Identifiers: chr17:g.7906877C>T (hg19) chr17:g.8003559C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8003559C>T , CM000679.2:g.8003559C>T GRCh38
NC_000017.10:g.7906877C>T , CM000679.1:g.7906877C>T GRCh37
NC_000017.9:g.7847602C>T NCBI36
NG_009092.1:g.5890C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.512C>T MANE Select ENSP00000254854.4:p.Ala171Val
ENST00000254854.4:c.512C>T ENSP00000254854.4:p.Ala171Val
NM_000180.3:c.512C>T NP_000171.1:p.Ala171Val
XM_011523816.1:c.512C>T XP_011522118.1:p.Ala171Val
NM_000180.4:c.512C>T MANE Select NP_000171.1:p.Ala171Val
Search 100 bp 5'
Search 100 bp 3'