Canonical Allele Identifier: CA672220124

Gene:

Linked Data

• dbSNP Id: rs1202509430
• MyVariant Identifiers: chr11:g.116313481A>T (hg19) ; chr11:g.116442764A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442764A>T , CM000673.2:g.116442764A>T	GRCh38
NC_000011.9:g.116313481A>T , CM000673.1:g.116313481A>T	GRCh37
NC_000011.8:g.115818691A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001748403.1:n.349+31113T>A