Canonical Allele Identifier: CA397952064
Gene: GUCY2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7915780C>A (hg19) chr17:g.8012462C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8012462C>A , CM000679.2:g.8012462C>A GRCh38
NC_000017.10:g.7915780C>A , CM000679.1:g.7915780C>A GRCh37
NC_000017.9:g.7856505C>A NCBI36
NG_009092.1:g.14793C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254854.5:c.1969C>A MANE Select ENSP00000254854.4:p.Leu657Met
ENST00000254854.4:c.1969C>A ENSP00000254854.4:p.Leu657Met
NM_000180.3:c.1969C>A NP_000171.1:p.Leu657Met
XM_011523816.1:c.1969C>A XP_011522118.1:p.Leu657Met
NM_000180.4:c.1969C>A MANE Select NP_000171.1:p.Leu657Met
Search 100 bp 5'
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