Canonical Allele Identifier: CA124924662
Gene:

Linked Data

ClinVar Variation Id: 1010420
ClinVar RCV Id: RCV003770608
dbSNP Id: rs978748301

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707437C>G , CM000667.2:g.112707437C>G GRCh38
NC_000005.9:g.112043134C>G , CM000667.1:g.112043134C>G GRCh37
NC_000005.8:g.112071033C>G NCBI36
NG_008481.4:g.19917C>G , LRG_130:g.19917C>G