Canonical Allele Identifier: CA283272998
Gene:

Linked Data

ClinVar Variation Id: 1330012
ClinVar RCV Id: RCV001801029
dbSNP Id: rs34149581

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737140T>C , CM000678.2:g.68737140T>C GRCh38
NC_000016.9:g.68771043T>C , CM000678.1:g.68771043T>C GRCh37
NC_000016.8:g.67328544T>C NCBI36
NG_008021.1:g.4849T>C , LRG_301:g.4849T>C