Canonical Allele Identifier: CA10576175
Gene:

Linked Data

ClinVar Variation Id: 226030
dbSNP Id: rs9923231

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31096368C>A , CM000678.2:g.31096368C>A GRCh38
NC_000016.9:g.31107689C>A , CM000678.1:g.31107689C>A GRCh37
NC_000016.8:g.31015190C>A NCBI36
NG_011564.1:g.3588G>T