Canonical Allele Identifier: CA828661857

Gene:

Linked Data

• dbSNP Id: rs1256654052
• gnomAD v3: 6-8169412-C-A
• gnomAD v4: 6-8169412-C-A
• MyVariant Identifiers: chr6:g.8169645C>A (hg19) ; chr6:g.8169412C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8169412C>A , CM000668.2:g.8169412C>A	GRCh38
NC_000006.11:g.8169645C>A , CM000668.1:g.8169645C>A	GRCh37
NC_000006.10:g.8114644C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926440.1:n.82+11152C>A
XR_926441.1:n.189+1492C>A
XR_926442.1:n.82+11152C>A
XR_926443.1:n.82+11152C>A
XR_001743950.1:n.179+1492C>A
XR_926440.2:n.74+11152C>A
XR_926441.2:n.179+1492C>A
XR_926443.2:n.83+11152C>A