Canonical Allele Identifier: CA290124710
Gene: CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1010294883
gnomAD v2: 17-34415371-C-T
gnomAD v3: 17-36088025-C-T
gnomAD v4: 17-36088025-C-T
MyVariant Identifiers: chr17:g.34415371C>T (hg19) chr17:g.36088025C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088025C>T , CM000679.2:g.36088025C>T GRCh38
NC_000017.10:g.34415371C>T , CM000679.1:g.34415371C>T GRCh37
NC_000017.9:g.31439484C>T NCBI36
NG_027730.1:g.7136G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001752857.1:n.1637-1521C>T
XR_001752858.1:n.673-1521C>T
XR_001752859.1:n.1584-1521C>T
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