Canonical Allele Identifier: CA292625004
Gene:

Linked Data

dbSNP Id: rs575751069
gnomAD v2: 17-55866222-A-T
gnomAD v3: 17-57788861-A-T
gnomAD v4: 17-57788861-A-T
MyVariant Identifiers: chr17:g.55866222A>T (hg19) chr17:g.57788861A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788861A>T , CM000679.2:g.57788861A>T GRCh38
NC_000017.10:g.55866222A>T , CM000679.1:g.55866222A>T GRCh37
NC_000017.9:g.53221221A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16665T>A
XR_934881.3:n.3815-16665T>A
Search 100 bp 5'
Search 100 bp 3'