Canonical Allele Identifier: CA323427621
Gene:

Linked Data

ClinVar Variation Id: 1211468
ClinVar RCV Id: RCV001583277
dbSNP Id: rs181069846

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474600T>C , CM000684.2:g.32474600T>C GRCh38
NC_000022.10:g.32870587T>C , CM000684.1:g.32870587T>C GRCh37
NC_000022.9:g.31200587T>C NCBI36
NG_016001.1:g.4881T>C
NG_016001.2:g.4881T>C