Canonical Allele Identifier: CA289293189
Gene:

Linked Data

dbSNP Id: rs934914756
MyVariant Identifiers: chr17:g.30237050C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237050C>T , CM000679.2:g.30237050C>T GRCh38
NC_000017.10:g.28564068C>T , CM000679.1:g.28564068C>T GRCh37
NC_000017.9:g.25588194C>T NCBI36
NG_011747.2:g.3887G>A

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.145C>T
XR_001752824.1:n.260C>T
Search 100 bp 5'
Search 100 bp 3'