Canonical Allele Identifier: CA828661872

Gene:

Linked Data

• dbSNP Id: rs1327332913
• MyVariant Identifiers: chr6:g.8169692G>A (hg19) ; chr6:g.8169459G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169459G>A , CM000668.2:g.8169459G>A	GRCh38
NC_000006.11:g.8169692G>A , CM000668.1:g.8169692G>A	GRCh37
NC_000006.10:g.8114691G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11199G>A
XR_926441.1:n.189+1539G>A
XR_926442.1:n.82+11199G>A
XR_926443.1:n.82+11199G>A
XR_001743950.1:n.179+1539G>A
XR_926440.2:n.74+11199G>A
XR_926441.2:n.179+1539G>A
XR_926443.2:n.83+11199G>A