Canonical Allele Identifier: CA566436776
Gene: IP6K3 HGNC NCBI

Linked Data

dbSNP Id: rs1249148919
gnomAD v2: 6-33716766-T-C
gnomAD v3: 6-33748989-T-C
gnomAD v4: 6-33748989-T-C
MyVariant Identifiers: chr6:g.33716766T>C (hg19) chr6:g.33748989T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33748989T>C , CM000668.2:g.33748989T>C GRCh38
NC_000006.11:g.33716766T>C , CM000668.1:g.33716766T>C GRCh37
NC_000006.10:g.33824744T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024446324.1:c.-309+3748A>G XP_024302092.1:n.-309+3748A>G
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