Canonical Allele Identifier: CA169367620
Gene: CNPY1 HGNC NCBI

Linked Data

dbSNP Id: rs536816944
gnomAD v2: 7-155285039-G-C
gnomAD v3: 7-155492344-G-C
gnomAD v4: 7-155492344-G-C
MyVariant Identifiers: chr7:g.155285039G>C (hg19) chr7:g.155492344G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155492344G>C , CM000669.2:g.155492344G>C GRCh38
NC_000007.13:g.155285039G>C , CM000669.1:g.155285039G>C GRCh37
NC_000007.12:g.154977800G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000635903.1:n.1217-8459C>G
ENST00000406197.5:c.*47+10677C>G ENSP00000384514.1:n.*47+10677C>G
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