Canonical Allele Identifier: CA663940261
Gene:

Linked Data

dbSNP Id: rs1334643111
MyVariant Identifiers: chr10:g.3409019G>A (hg19) chr10:g.3366827G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366827G>A , CM000672.2:g.3366827G>A GRCh38
NC_000010.10:g.3409019G>A , CM000672.1:g.3409019G>A GRCh37
NC_000010.9:g.3399019G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47971G>A
Search 100 bp 5'
Search 100 bp 3'