Canonical Allele Identifier: CA783230569

Gene:

Linked Data

• dbSNP Id: rs1359200250
• MyVariant Identifiers: chr19:g.11071337C>T (hg19) ; chr19:g.10960661C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10960661C>T , CM000681.2:g.10960661C>T	GRCh38
NC_000019.9:g.11071337C>T , CM000681.1:g.11071337C>T	GRCh37
NC_000019.8:g.10932337C>T	NCBI36
NG_011556.2:g.4740C>T
NG_011556.3:g.4730C>T