Canonical Allele Identifier: CA427349348
Gene:

Linked Data

dbSNP Id: rs1440199505
MyVariant Identifiers: chr2:g.88315875C>T (hg19) chr2:g.88016356C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016356C>T , CM000664.2:g.88016356C>T GRCh38
NC_000002.11:g.88315875C>T , CM000664.1:g.88315875C>T GRCh37
NC_000002.10:g.88096990C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.701C>T
XR_940336.3:n.701C>T
Search 100 bp 5'
Search 100 bp 3'