Canonical Allele Identifier: CA292625010
Gene:

Linked Data

dbSNP Id: rs1004446095
gnomAD v2: 17-55866262-C-T
gnomAD v3: 17-57788901-C-T
gnomAD v4: 17-57788901-C-T
MyVariant Identifiers: chr17:g.55866262C>T (hg19) chr17:g.57788901C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788901C>T , CM000679.2:g.57788901C>T GRCh38
NC_000017.10:g.55866262C>T , CM000679.1:g.55866262C>T GRCh37
NC_000017.9:g.53221261C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16705G>A
XR_934881.3:n.3815-16705G>A
Search 100 bp 5'
Search 100 bp 3'