Canonical Allele Identifier: CA336266039
Gene:

Linked Data

ClinVar Variation Id: 439468
ClinVar RCV Id: RCV000506423
dbSNP Id: rs184119101

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648060A>C , CM000685.2:g.136648060A>C GRCh38
NC_000023.10:g.135730219A>C , CM000685.1:g.135730219A>C GRCh37
NC_000023.9:g.135557885A>C NCBI36
NG_007280.1:g.4884A>C , LRG_141:g.4884A>C