Canonical Allele Identifier: CA624868013
Gene: GUCY2D HGNC NCBI

Linked Data

dbSNP Id: rs1279662927
gnomAD v2: 17-7919020-G-C
gnomAD v4: 17-8015702-G-C
MyVariant Identifiers: chr17:g.7919020G>C (hg19) chr17:g.8015702G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8015702G>C , CM000679.2:g.8015702G>C GRCh38
NC_000017.10:g.7919020G>C , CM000679.1:g.7919020G>C GRCh37
NC_000017.9:g.7859745G>C NCBI36
NG_009092.1:g.18033G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000254854.5:c.2945-41G>C MANE Select ENSP00000254854.4:n.2945-41G>C
ENST00000254854.4:c.2945-41G>C ENSP00000254854.4:n.2945-41G>C
NM_000180.3:c.2945-41G>C NP_000171.1:n.2945-41G>C
XM_011523816.1:c.2945-41G>C XP_011522118.1:n.2945-41G>C
NM_000180.4:c.2945-41G>C MANE Select NP_000171.1:n.2945-41G>C
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