Canonical Allele Identifier: CA625447412
Gene:

Linked Data

dbSNP Id: rs1372006683
gnomAD v2: 17-28564184-G-A
gnomAD v3: 17-30237166-G-A
gnomAD v4: 17-30237166-G-A
MyVariant Identifiers: chr17:g.28564184G>A (hg19) chr17:g.30237166G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237166G>A , CM000679.2:g.30237166G>A GRCh38
NC_000017.10:g.28564184G>A , CM000679.1:g.28564184G>A GRCh37
NC_000017.9:g.25588310G>A NCBI36
NG_011747.2:g.3771C>T

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+96G>A
XR_001752824.1:n.280+96G>A
Search 100 bp 5'
Search 100 bp 3'