Canonical Allele Identifier: CA915943573
Gene:

Linked Data

ClinVar Variation Id: 657695
ClinVar RCV Id: RCV003536027
dbSNP Id: rs1580995582

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707427C>T , CM000667.2:g.112707427C>T GRCh38
NC_000005.9:g.112043124C>T , CM000667.1:g.112043124C>T GRCh37
NC_000005.8:g.112071023C>T NCBI36
NG_008481.4:g.19907C>T , LRG_130:g.19907C>T