Canonical Allele Identifier: CA12321089
Gene:

Linked Data

ClinVar Variation Id: 694519
ClinVar RCV Id: RCV000856579
dbSNP Id: rs2763979

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31826815C>T , CM000668.2:g.31826815C>T GRCh38
NC_000006.11:g.31794592C>T , CM000668.1:g.31794592C>T GRCh37
NC_000006.10:g.31902571C>T NCBI36