Canonical Allele Identifier: CA13844405
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 511090
ClinVar RCV Id: RCV000605277
dbSNP Id: rs6311

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897343C>T , CM000675.2:g.46897343C>T GRCh38
NC_000013.10:g.47471478C>T , CM000675.1:g.47471478C>T GRCh37
NC_000013.9:g.46369479C>T NCBI36
NG_013011.1:g.4692G>A