Canonical Allele Identifier: CA230924494

Gene:

Linked Data

• dbSNP Id: rs895685955
• MyVariant Identifiers: chr11:g.128325355C>T (hg19) ; chr11:g.128455460C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455460C>T , CM000673.2:g.128455460C>T	GRCh38
NC_000011.9:g.128325355C>T , CM000673.1:g.128325355C>T	GRCh37
NC_000011.8:g.127830565C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4180C>T
XR_948165.1:n.3467+713C>T