Canonical Allele Identifier: CA817908533

Gene:

Linked Data

• dbSNP Id: rs1191659610
• MyVariant Identifiers: chr6:g.11943858A>C (hg19) ; chr6:g.11943625A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943625A>C , CM000668.2:g.11943625A>C	GRCh38
NC_000006.11:g.11943858A>C , CM000668.1:g.11943858A>C	GRCh37
NC_000006.10:g.12051844A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-7910A>C