Canonical Allele Identifier: CA828661883

Gene:

Linked Data

• dbSNP Id: rs1273985265
• MyVariant Identifiers: chr6:g.8169759T>C (hg19) ; chr6:g.8169526T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169526T>C , CM000668.2:g.8169526T>C	GRCh38
NC_000006.11:g.8169759T>C , CM000668.1:g.8169759T>C	GRCh37
NC_000006.10:g.8114758T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11266T>C
XR_926441.1:n.189+1606T>C
XR_926442.1:n.82+11266T>C
XR_926443.1:n.82+11266T>C
XR_001743950.1:n.179+1606T>C
XR_926440.2:n.74+11266T>C
XR_926441.2:n.179+1606T>C
XR_926443.2:n.83+11266T>C