Canonical Allele Identifier: CA12231312
Gene:

Linked Data

ClinVar Variation Id: 12389
dbSNP Id: rs1799724

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31574705C>T , CM000668.2:g.31574705C>T GRCh38
NC_000006.11:g.31542482C>T , CM000668.1:g.31542482C>T GRCh37
NC_000006.10:g.31650461C>T NCBI36
NG_007462.1:g.4133C>T
NG_012010.1:g.7607C>T