Canonical Allele Identifier: CA308886486
Gene:

Linked Data

ClinVar Variation Id: 1197019
ClinVar RCV Id: RCV001560704
dbSNP Id: rs117656888

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909484C>G , CM000681.2:g.44909484C>G GRCh38
NC_000019.9:g.45412741C>G , CM000681.1:g.45412741C>G GRCh37
NC_000019.8:g.50104581C>G NCBI36
NG_007084.2:g.8703C>G