Canonical Allele Identifier: CA134173726

Gene:

Linked Data

• dbSNP Id: rs954327327
• MyVariant Identifiers: chr6:g.11943949A>G (hg19) ; chr6:g.11943716A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943716A>G , CM000668.2:g.11943716A>G	GRCh38
NC_000006.11:g.11943949A>G , CM000668.1:g.11943949A>G	GRCh37
NC_000006.10:g.12051935A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-7819A>G