Canonical Allele Identifier: CA135813142
Gene: ZKSCAN8P1 HGNC NCBI

Linked Data

dbSNP Id: rs187855697
gnomAD v2: 6-28129850-A-G
gnomAD v3: 6-28162072-A-G
gnomAD v4: 6-28162072-A-G
MyVariant Identifiers: chr6:g.28129850A>G (hg19) chr6:g.28162072A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.28162072A>G , CM000668.2:g.28162072A>G GRCh38
NC_000006.11:g.28129850A>G , CM000668.1:g.28129850A>G GRCh37
NC_000006.10:g.28237829A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000562227.2:n.53+251A>G
ENST00000440790.6:n.41+251A>G
ENST00000570126.1:n.30+251A>G
NR_103448.1:n.61+251A>G
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