Canonical Allele Identifier: CA287548472
Gene:

Linked Data

dbSNP Id: rs1027281572
MyVariant Identifiers: chr17:g.8040626C>A (hg19) chr17:g.8137308C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137308C>A , CM000679.2:g.8137308C>A GRCh38
NC_000017.10:g.8040626C>A , CM000679.1:g.8040626C>A GRCh37
NC_000017.9:g.7981351C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1541C>A
XR_934203.1:n.70-2169C>A
XR_934202.2:n.414-1541C>A
Search 100 bp 5'
Search 100 bp 3'