Canonical Allele Identifier: CA49690023
Gene:

Linked Data

dbSNP Id: rs887749502
MyVariant Identifiers: chr2:g.70872873T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70872873T>C , CM000664.2:g.70872873T>C GRCh38
NC_000002.11:g.71100003T>C , CM000664.1:g.71100003T>C GRCh37
NC_000002.10:g.70953511T>C NCBI36