Canonical Allele Identifier: CA230924502

Gene:

Linked Data

• dbSNP Id: rs988825993
• MyVariant Identifiers: chr11:g.128325426C>T (hg19) ; chr11:g.128455531C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455531C>T , CM000673.2:g.128455531C>T	GRCh38
NC_000011.9:g.128325426C>T , CM000673.1:g.128325426C>T	GRCh37
NC_000011.8:g.127830636C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4251C>T
XR_948165.1:n.3467+784C>T