Canonical Allele Identifier: CA700075512

Gene:

Linked Data

• dbSNP Id: rs1192348283
• MyVariant Identifiers: chr13:g.66211995T>G (hg19) ; chr13:g.65637863T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.65637863T>G , CM000675.2:g.65637863T>G	GRCh38
NC_000013.10:g.66211995T>G , CM000675.1:g.66211995T>G	GRCh37
NC_000013.9:g.65109996T>G	NCBI36