Canonical Allele Identifier: CA448417765

Gene:

Linked Data

• dbSNP Id: rs1581439057
• MyVariant Identifiers: chr6:g.11943548G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943315G>A , CM000668.2:g.11943315G>A	GRCh38
NC_000006.11:g.11943548G>A , CM000668.1:g.11943548G>A	GRCh37
NC_000006.10:g.12051534G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-8220G>A