Canonical Allele Identifier: CA222002616
Gene:

Linked Data

dbSNP Id: rs964647811
MyVariant Identifiers: chr11:g.45528064G>A (hg19) chr11:g.45506514G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506514G>A , CM000673.2:g.45506514G>A GRCh38
NC_000011.9:g.45528064G>A , CM000673.1:g.45528064G>A GRCh37
NC_000011.8:g.45484640G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16743C>T
XR_931245.3:n.566-16743C>T
Search 100 bp 5'
Search 100 bp 3'