Canonical Allele Identifier: CA698193332

Gene:

Linked Data

• dbSNP Id: rs1377179936
• MyVariant Identifiers: chr13:g.43135259A>G (hg19) ; chr13:g.42561123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42561123A>G , CM000675.2:g.42561123A>G	GRCh38
NC_000013.10:g.43135259A>G , CM000675.1:g.43135259A>G	GRCh37
NC_000013.9:g.42033259A>G	NCBI36
NG_008990.1:g.3388A>G