Canonical Allele Identifier: CA830285526
Gene:

Linked Data

dbSNP Id: rs1172271898
MyVariant Identifiers: chr6:g.98550267G>A (hg19) chr6:g.98102391G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102391G>A , CM000668.2:g.98102391G>A GRCh38
NC_000006.11:g.98550267G>A , CM000668.1:g.98550267G>A GRCh37
NC_000006.10:g.98656988G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3121G>A
XR_942809.1:n.456+3121G>A
Search 100 bp 5'
Search 100 bp 3'