Canonical Allele Identifier: CA625447489
Gene:

Linked Data

dbSNP Id: rs1225864485
gnomAD v2: 17-28564355-A-T
gnomAD v3: 17-30237337-A-T
gnomAD v4: 17-30237337-A-T
MyVariant Identifiers: chr17:g.28564355A>T (hg19) chr17:g.30237337A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237337A>T , CM000679.2:g.30237337A>T GRCh38
NC_000017.10:g.28564355A>T , CM000679.1:g.28564355A>T GRCh37
NC_000017.9:g.25588481A>T NCBI36
NG_011747.2:g.3600T>A

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+267A>T
XR_001752824.1:n.280+267A>T
Search 100 bp 5'
Search 100 bp 3'