Canonical Allele Identifier: CA289293179
Gene:

Linked Data

dbSNP Id: rs926160922
gnomAD v2: 17-28564063-C-A
gnomAD v3: 17-30237045-C-A
gnomAD v4: 17-30237045-C-A
MyVariant Identifiers: chr17:g.28564063C>A (hg19) chr17:g.30237045C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237045C>A , CM000679.2:g.30237045C>A GRCh38
NC_000017.10:g.28564063C>A , CM000679.1:g.28564063C>A GRCh37
NC_000017.9:g.25588189C>A NCBI36
NG_011747.2:g.3892G>T

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.140C>A
XR_001752824.1:n.255C>A
Search 100 bp 5'
Search 100 bp 3'