Canonical Allele Identifier: CA497953220
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915566C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012248C>G , CM000679.2:g.8012248C>G GRCh38
NC_000017.10:g.7915566C>G , CM000679.1:g.7915566C>G GRCh37
NC_000017.9:g.7856291C>G NCBI36
NG_009092.1:g.14579C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1854C>G MANE Select ENSP00000254854.4:p.Val618=
ENST00000254854.4:c.1854C>G ENSP00000254854.4:p.Val618=
NM_000180.3:c.1854C>G NP_000171.1:p.Val618=
XM_011523816.1:c.1854C>G XP_011522118.1:p.Val618=
NM_000180.4:c.1854C>G MANE Select NP_000171.1:p.Val618=
Search 100 bp 5'
Search 100 bp 3'